Studied for
3 endpoints · 6 findings · 4 papers
- Vertebral fracture incidencelowersEvidence strength: moderate. Human evidence with one recorded weakness, or capped at moderate by its design or by unread numbers.
- WOMAC pain subscalelowersEvidence strength: moderate. Human evidence with one recorded weakness, or capped at moderate by its design or by unread numbers.
- Non-vertebral fracture incidencelowersEvidence strength: limited. Human evidence with several recorded weaknesses, or a design that tops out at limited.
What the evidence says
How to read these marks6 findings · 3 endpoints · 4 papers · by evidence strength
What moved
6 findings
Decreases vertebral fracture incidence
ModerateEvidence strength: moderate. Human evidence with one recorded weakness, or capped at moderate by its design or by unread numbers.Findingreplicated ×2“Strontium ranelate was associated with a reduction in the relative risk of vertebral fracture, relative to placebo, of 40% (RR = 0.60, 95% CI [0.53–0.70], p < 0.001).”
Quoted verbatim from Vertebral anti-fracture efficacy of strontium ranelate according to pre-treatment bone turnover.. - Study
- RCT
- Dose
- strontium ranelate 2 g/day
- Population
- Post-menopausal women with osteoporosis, pooled from the SOTI and TROPOS randomised placebo-controlled trials; calcium and vitamin D supplements given to both arms; 3-year vertebral fracture data
Effect 0.6 risk ratio, 95% CI 0.53 to 0.7
Vertebral anti-fracture efficacy of strontium ranelate according to pre-treatment bone turnover.2010PMID:19436941Permalink
Decreases WOMAC pain subscale
ModerateEvidence strength: moderate. Human evidence with one recorded weakness, or capped at moderate by its design or by unread numbers.Finding“Treatment with strontium ranelate 2 g/day was associated with significantly lower WOMAC total score (p=0.045) and pain subscore (p=0.028), and a trend toward lower physical function subscore (p=0.099) and global knee pain (p=0.065) (table 2).”
Quoted verbatim from Efficacy and safety of strontium ranelate in the treatment of knee osteoarthritis: results of a double-blind, randomised placebo-controlled trial.. - Study
- RCT
- Dose
- strontium ranelate 2 g/day
- Population
- Outpatients aged 50 or over with knee osteoarthritis (Kellgren and Lawrence grade 2 or 3), intention-to-treat population; 2 g/day dose stratum only (the 1 g/day dose showed no significant reduction)
Efficacy and safety of strontium ranelate in the treatment of knee osteoarthritis: results of a double-blind, randomised placebo-controlled trial.2013PMID:23117245Permalink
Decreases vertebral fracture incidence
LimitedEvidence strength: limited. Human evidence with several recorded weaknesses, or a design that tops out at limited.Findingreplicated ×2“The cumulative incidence of new vertebral fractures in the 10-year population in years 6 to 10 was significantly lower than that observed over 5 years in the FRAX®-matched placebo population (20.6 ± 3.0% versus 28.2 ± 2.4%, respectively; relative reduction in risk [RRR] 35%, P = 0.016).”
Quoted verbatim from Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis.. - Study
- cohort
- Dose
- strontium ranelate 2 g/day
- Population
- Postmenopausal women with osteoporosis who took strontium ranelate for up to 10 years in the open-label extension of SOTI and TROPOS (the 10-year population, completers only), compared in years 6 to 10 with a FRAX-matched placebo group drawn from the TROPOS placebo arm over years 0 to 5; calcium and vitamin D given
Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis.2012PMID:22124575Permalink
Decreases non-vertebral fracture incidence
LimitedEvidence strength: limited. Human evidence with several recorded weaknesses, or a design that tops out at limited.Findingreplicated ×1“Similarly, the 10-year population had significantly lower rates of nonvertebral fracture and new osteoporotic fracture in years 6 to 10 than the FRAX®-matched placebo population over 5 years (nonvertebral fracture: 13.7 ± 2.3% versus 20.2 ± 2.2%, respectively, RRR 38%, P = 0.023; new osteoporotic fracture: 30.3 ± 3.1% versus 39.2 ± 2.5%, RRR 30%, P = 0.012).”
Quoted verbatim from Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis.. - Study
- cohort
- Dose
- strontium ranelate 2 g/day
- Population
- Postmenopausal women with osteoporosis who took strontium ranelate for up to 10 years in the open-label extension of SOTI and TROPOS (the 10-year population, completers only), compared in years 6 to 10 with a FRAX-matched placebo group drawn from the TROPOS placebo arm over years 0 to 5; calcium and vitamin D given
Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis.2012PMID:22124575Permalink
Decreases vertebral fracture incidence
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Findingreplicated ×2“A 37% reduction in vertebral fractures (RR 0.63, 95% CI 0.56, 0.71) and a 14% reduction in non-vertebral fractures (RR 0.86, 95% CI 0.75, 0.98) were demonstrated over three years with 2 g of strontium ranelate daily in a treatment population.”
Quoted verbatim from Strontium ranelate for preventing and treating postmenopausal osteoporosis.. - Study
- meta-analysis
- Dose
- strontium ranelate 2 g daily
- Population
- Postmenopausal women with osteoporosis (treatment population: prevalent vertebral fractures and/or lumbar spine BMD T score below -2.5 SD); pooled RCTs of strontium ranelate versus placebo; 2 g daily dose stratum, three years
Effect 0.63 risk ratio, 95% CI 0.56 to 0.71
Strontium ranelate for preventing and treating postmenopausal osteoporosis.2006PMID:17054253Permalink
Decreases non-vertebral fracture incidence
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Findingreplicated ×1“A 37% reduction in vertebral fractures (RR 0.63, 95% CI 0.56, 0.71) and a 14% reduction in non-vertebral fractures (RR 0.86, 95% CI 0.75, 0.98) were demonstrated over three years with 2 g of strontium ranelate daily in a treatment population.”
Quoted verbatim from Strontium ranelate for preventing and treating postmenopausal osteoporosis.. - Study
- meta-analysis
- Dose
- strontium ranelate 2 g daily
- Population
- Postmenopausal women with osteoporosis (treatment population: prevalent vertebral fractures and/or lumbar spine BMD T score below -2.5 SD); pooled RCTs of strontium ranelate versus placebo; 2 g daily dose stratum, three years
Effect 0.86 risk ratio, 95% CI 0.75 to 0.98
Strontium ranelate for preventing and treating postmenopausal osteoporosis.2006PMID:17054253Permalink
On the label
Labelled products
120 products
Source: NIH DSLD · Ingredient: strontium(2+) · 120 products · Declared amount per serving: 0.25–2,000 mg (109 products)
120 labels state an amount0 do not
- Advanced BionutritionalsUltimate Bone SupportStrontium Citrate · Strontium (Form: as Strontium Citrate)500 mgper 2 Tablet(s)DSLD:12885
- Advanced Nutrition by ZahlerBoneFactorStrontium Citrate100 mgper 4 Tablet(s)DSLD:301092
- Advanced Nutrition by ZahlerPowerCal 1000 mgStrontium Citrate650 mgper 2 Tablet(s)DSLD:301106
- Advanced Nutrition by ZahlerPowerCal 900 mgStrontium Citrate40 mgper 2 Capsule(s)DSLD:260277
- Allergy Research GroupOsteo-Vi-MinStrontium Carbonate · Strontium (Form: as Strontium Carbonate)5 mgper 3.5 Gram(s)DSLD:233530
- Allergy Research GroupOsteo-Vi-MinStrontium Chloride · Strontium (Form: as Strontium Chloride)2.5 mgper 2 Tablet(s)DSLD:233538
- AOR Advanced Orthomolecular Research PremiumStrontium Support IIStrontium Citrate · Strontium (Form: from Strontium Citrate)682 mgper 1 Capsule(s)DSLD:214871
- Best NaturalsStrontium 680 mgStrontium Citrate680 mgper 2 Capsule(s)DSLD:270125
- Beyond HealthBone Mineral FormulaStrontium Gluconate50 mgper 4 Tablet(s)DSLD:306878
- Bio-Tech PharmacalStrontiumStrontium Citrate · Strontium (Form: as Strontium Citrate)300 mgper 1 Capsule(s)DSLD:217212
- BioSchwartzBone StrengthStrontium Citrate3 mgper 4 Capsule(s)DSLD:249862
- Body Dynamics MaXzorbceuticals NutritionJoint RenewalStrontium Citrate · Strontium (Form: as Strontium Citrate)33 mgper 6 Capsule(s)DSLD:292662
Show the remaining 108
- CodeageLiposomal Strontiumfrom680 mgper 3 Capsule(s)DSLD:333433
- Doctor's BestStrontium Bone Maker 340 mgStrontium Note: elemental680 mgper 2 Capsule(s)DSLD:25016
- Doctor's BestStrontium Bone Maker 340 mgStrontium Note: elemental680 mgper 2 Capsule(s)DSLD:62598
- Doctor's BestStrontium Bone Maker 340 mgStrontium Citrate · Strontium (Form: from Strontium Citrate) Note: elemental680 mgper 2 Capsule(s)DSLD:62637
- Doctor's BestStrontium Bone Maker 340 mgStrontium Citrate · Strontium (Form: from Strontium Citrate) Note: elemental680 mgper 2 Veggie Capsule(s)DSLD:62638
- Douglas LaboratoriesOsteo-Support FormulaStrontium Citrate · Strontium (Form: as Strontium Citrate)7.5 mcgper 3 Tablet(s)DSLD:244647
- Douglas LaboratoriesStrontiumStrontium Citrate · Strontium (Form: as Strontium Citrate)200 mgper 1 Vegetarian Capsule(s)DSLD:274098
- Dr. MercolaBone Support with Strontium & BoronStrontium Citrate · Strontium (Form: from Strontium Citrate)500 mgper 2 Capsule(s)DSLD:250320
- EuroMedicaStrontiumStrontium Citrate680 mgper 2 Capsule(s)DSLD:309452
- Garden of Life MyKind OrganicsOrganic Plant CalciumAlgae · from organic algae4 mgper 1 Tablet(s)DSLD:327404
- Garden of Life MyKind OrganicsOrganic Plant CalciumAlgae · organic algae4 mgper 3 Tablet(s)DSLD:329093
- Garden of Life Vitamin CodeGrowth FactorsStrontium Citrate · elemental680 mgper 3 Capsule(s)DSLD:327400
- Garden of Life Vitamin CodeRaw CalciumAlgae · naturally occurring3.8 mgper 2 Capsule(s)DSLD:321391
- Garden of Life Vitamin CodeRaw CalciumAlgae · naturally occurring3.8 mgper 2 Capsule(s)DSLD:321392
- Garden of Life Vitamin CodeRaw CalciumAlgae · naturally occurring from algae3.8 mgper 4 Capsule(s)DSLD:326771
- Garden of Life Vitamin CodeVitamin Code Grow Bone CalciumAlgae · naturally occurring3.8 mgper 2 Capsule(s)DSLD:321384
- Garden of Life Vitamin Code Raw CalciumAlgae3.8 mgper 2 Capsule(s)DSLD:273843
- Good StateDigital Liquid120 mcgper 2 mLDSLD:310820
- Good StateDigital Liquid1 mgper 4.17 mLDSLD:310821
- Good StateDigital Liquid250 mcgper 4.17 mLDSLD:310822
- Good StateIonic ManStrontium Chloride0.25 mgper 4.17 mLDSLD:310829
- Good StateIonic Man (Men's Multi)Strontium Chloride1 mgper 4.17 mLDSLD:310830
- Good StateIonic Strontium 60,000 PPMStrontium Chloride30 mgper 0.5 mLDSLD:276971
- Good StateIonic WomanStrontium Chloride1 mgper 4.17 mLDSLD:310841
- Good StateIonic WomanStrontium Chloride0.25 mgper 4.17 mLDSLD:310842
- hank & brian'sbone jour!Strontium Citrate · Strontium (Form: from Strontium Citrate)600 mcgper 4 Capsule(s)DSLD:254894
- Harmonic InnerprizesCalMag Skeletal RejuvenatorStrontium Citrate150 mgper 1 Capsule(s)DSLD:213002
- Harmonic InnerprizesCalMag Skeletal RejuvenatorStrontium Citrate150 mgper 6 Capsule(s)DSLD:81544
- HD MuscleVitaHD Essential Health MultiStrontium Citrate · Strontium (Form: as Strontium Citrate)250 mgper 5 Capsule(s)DSLD:245711
- Health ConcernsBioStrongStrontium Carbonate680 mgper 2 Capsule(s)DSLD:259215
- Health Products DistributorsBone GuardianStrontium Citrate · Strontium (Form: from Strontium Citrate)500 mcgper 6 Tablet(s)DSLD:254891
- Highland LaboratoriesStronium Bone PowerStrontium Citrate · Strontium (Form: from Strontium Citrate)350 mgper 1 Vegetarian Capsule(s)DSLD:79550
- HoltraCeuticalsBone RestoreStrontium Carbonate · Strontium (Form: from strontium carbonate)1,000 mgper 4 Capsule(s)DSLD:270858
- Integrative TherapeuticsOsteoprime ForteStrontium Citrate Complex2 mgper 4 Capsule(s)DSLD:317371
- Integrative TherapeuticsOsteoprime UltraStrontium Citrate · strontium citrate complex6 mgper 4 Tablet(s)DSLD:328349
- JuvenonUltimate Bone Density2,000 mgper 2 Tablet(s)DSLD:66803
- KidzPlayBonez PlayStrontium Citrate · Strontium (Form: {Strontium} Citrate, & {Strontium} Malate)9.6 mgper 1 tspDSLD:22523
- Klaire LabsStrontium 300 mgStrontium Citrate300 mgper 1 Capsule(s)DSLD:264969
- Klaire LabsStrontium 300 mgStrontium Citrate · strontium citrate complex300 mgper 1 Capsule(s)DSLD:322457
- Life ExtensionStrontium Caps 750 mgStrontium Citrate · Strontium (Form: as Strontium Citrate)750 mgper 3 Vegetarian Capsule(s)DSLD:231914
- Life ExtensionStrontium Caps 750 mgStrontium Citrate750 mgper 3 Vegetarian Capsule(s)DSLD:328714
- LifeSeasons TherapeuticsBone Densi-TStrontium Citrate2.45 mgper 4 Capsule(s)DSLD:310465
- Martin Avenue PharmacyBone Total HealthStrontium Aspartate · Strontium (Form: from Strontium Aspartate)10 mcgper 4 Tablet(s)DSLD:18801
- Moss NutritionOsteoSelectStrontium Citrate · Strontium (Form: as Strontium Citrate)50 mgper 4 Tablet(s)DSLD:275536
- Moss NutritionOsteoSelectStrontium Citrate50 mgper 4 Tablet(s)DSLD:334945
- Natural ClinicianClinical Osteoporosis Support8 mcgper 2 Capsule(s)DSLD:18651
- Nature's WayAlive! Calcium 1,200 mgAquamin calcified mineral source Red Algae8 mgper 2 Tablet(s)DSLD:328096
- Nature's WayAlive! Calcium 1,200 mgAquamin · calcified mineral source8 mgper 2 Tablet(s)DSLD:332962
- Nature's WayAlive! Calcium 1,200 mgAquamin calcified mineral source Red Algae8 mgper 2 Tablet(s)DSLD:333868
- Nature's WayAlive! Calcium Bone SupportAquamin · calcified mineral source8 mgper 2 Tablet(s)DSLD:332961
- Nature's WayAlive! Calcium Bone Support 1,200 mgAquamin · calcified mineral source red algae8 mgper 2 Tablet(s)DSLD:333700
- Nature's WayOsteoPrimeStrontium Citrate · strontium citrate complex2 mgper 2 Capsule(s)DSLD:328135
- New ChapterBone Strength Take CareAlgae · Strontium (Form: from Algae Genus: Algas Species: calcareas)5 mgper 3 Tablet(s)DSLD:2395
- New ChapterBone Strength Take CareAlgae · Strontium (Form: from Algae Genus: Algas Species: calcareas)5 mgper 3 Tablet(s)DSLD:2396
- New ChapterBone Strength Take Care Slim TabletsAlgae · Organic Algae5.5 mgper 3 Tablet(s)DSLD:288192
- New ChapterBone Strength Take Care Slim TabletsAlgae Lithothamnion calcareum · From organic algae5.5 mgper 3 Tablet(s)DSLD:294134
- New ChapterBone Strength Take Care Slim Tabsalgae Lithothamnion · organic algae Lithothamnion5.5 mgper 3 Tablet(s)DSLD:294135
- New ChapterBone Strength Take Care Slim Tabsalgae Lithothamnion · organic algae Lithothamnion5.5 mgper 3 Tablet(s)DSLD:294136
- New ChapterBone Strength Take Care Slim Tabsalgae Lithothamnion · Organic algae5.5 mgper 3 Tablet(s)DSLD:294137
- New ChapterBone Strength Take Care Slim TabsAlgae · Strontium (Form: from Algae (Form: Lithothamnion calcareum Genus: Lithothamnion Species: calcareum, & Lithothamnion corallioides Genus: Lithothamnion Species: corallioides))5 mgper 3 Tablet(s)DSLD:82694
- New ChapterBone Strength Take Care Tiny TabsAlgae Lithothamnion calcareum · Strontium (Form: from Algae Lithothamnion calcareum Genus: Lithothamnion Species: calcareum, & Algae Lithothamnion corallioides Genus: Lithothamnion Species: corallioides)5 mgper 6 Tablet(s)DSLD:202137
- New ChapterBone Strength Take Care Tiny Tabsalgae Lithothamnion5.5 mgper 6 Tablet(s)DSLD:294138
- New ChapterBone Strength Take Care Tiny TabsAlgae · Strontium (Form: from Algae (Form: Lithothamnion calcareum Genus: Lithothamnion Species: calcareum, & {Lithothamnion} corallioides Genus: Lithothamnion Species: corallioides))5 mgper 6 Tablet(s)DSLD:38446
- New ChapterOrganic Plant Calcium Women Under 40Algae Lithothamnion · organic3.7 mgper 2 Tablet(s)DSLD:326599
- NuMedicaOsteoV SCStrontium Citrate · Strontium (Form: as Strontium Citrate)680 mgper 3 Capsule(s)DSLD:217504
- NuMedicaOsteoV SCStrontium Citrate680 mgper 3 Capsule(s)DSLD:323670
- NusaPureStrontium Citrate 680 mg680 mgper 2 Veg Capsule(s)DSLD:247044
- NutraChampsBone StrengthStrontium Citrate10 mgper 4 Capsule(s)DSLD:338083
- Nutri-WestTotal CalciumStrontium Chloride · Strontium (Form: as {strontium} chelate)50 mcgper 1 Tablet(s)DSLD:28421
- NutriCologyOsteo-Vi-MinStrontium Chloride · Strontium (Form: as Strontium Chloride)5 mgper 1 tspDSLD:235594
- NutriCologyOsteo-Vi-MinStrontium Chloride · Strontium (Form: as Strontium Chloride)5 mgper 1 tspDSLD:235595
- NutriCologyOsteo-Vi-MinStrontium Carbonate · Strontium (Form: as Strontium Carbonate)2.5 mgper 2 Tablet(s)DSLD:235607
- NutriCologyOsteo-Vi-MinStrontium Chloride · Strontium (Form: as Strontium Chloride)2.5 mgper 2 Tablet(s)DSLD:235609
- OnnitDay Pack: Stron Bone227 mgper 1 Tablet(s)DSLD:67382
- OnnitStron BoneStrontium Citrate680 mgper 3 Capsule(s)DSLD:256700
- OnnitStron BoneStrontium Citrate · Strontium (Form: as Strontium Citrate)680 mgper 3 Tablet(s)DSLD:64595
- OnnitStronBone26 mgper 1 Packet(s)DSLD:273123
- Ortho Molecular ProductsStrontium950 mgper 1 Capsule(s)DSLD:174420
- PerqueBone Guard Forte 20 TabsulesStrontium Gluconate · Strontium (Form: as {strontium} gluconate)50 mgper 2 Capsule(s)DSLD:18701
- PerqueBone Guard Forte 20 TabsulesStrontium Gluconate · Strontium (Form: as {strontium} gluconate)50 mgper 2 Capsule(s)DSLD:18708
- PerqueBone Guard Forte TabsulesStrontium Citrate · Strontium (Form: as Strontium Citrate)50 mgper 4 Tabsule(s)DSLD:240635
- PerqueBone Guard Forte TabsulesStrontium Citrate · Strontium (Form: as Strontium Citrate)50 mgper 4 Tabsule(s)DSLD:240637
- PerqueHair, Skin, & Nails GuardStrontium Citrate · Strontium (Form: as Strontium Citrate)50 mgper 4 Tabsule(s)DSLD:240760
- PlantFusionVegan Plant-Based Calcium 1,000 mgAquamin7 mgper 3 Tablet(s)DSLD:261967
- Progressive Professional from Progressive LaboratoriesOsteo-Mins AMStrontium Citrate500 mgper 2 Capsule(s)DSLD:263016
- Pure EncapsulationsStrontium (Citrate)Strontium Citrate · Strontium (Form: as Strontium Citrate)227 mgper 1 Capsule(s)DSLD:185255
- Pure EncapsulationsStrontium (Citrate)Strontium Citrate · Strontium (Form: as Strontium Citrate)227 mgper 1 Capsule(s)DSLD:278363
- SolarayStrontium Citrate 250 mgStrontium Citrate250 mgper 1 VegCap(s)DSLD:338717
- SuperSmartSuper Bone Formula96 mgper 4 Tablet(s)DSLD:332500
- SwansonStrontium Citrate 340 mgStrontium Citrate340 mgper 1 Capsule(s)DSLD:273548
- Systemic Formulas Bio NutrimentCalMDLQStrontium Citrate · Strontium (Form: {Strontium} Citrate, & {Strontium} Malate)9.6 mgper 15 mLDSLD:22114
- Terry NaturallyStrontiumStrontium Citrate · Strontium (Form: from Strontium Citrate)680 mgper 2 Capsule(s)DSLD:202434
- ThompsonIdeal Bone FormulaStrontium Chloride · Strontium (Form: as Strontium Chloride)254 mcgper 4 Capsule(s)DSLD:36497
- tnvitaminsStrontium Citrate 340 mgStrontium Citrate · Strontium (Form: from Strontium Citrate)680 mgper 1 Quick Release Capsule(s)DSLD:217851
- tnvitaminsStrontium Citrate 680 mgStrontium Citrate680 mgper 1 Capsule(s)DSLD:276883
- Trace Minerals ResearchIonic Strontium 100 mgStrontium Chloride · Strontium (Form: as Strontium Chloride)100 mgper 1.25 mLDSLD:78971
- Traditional NutritionalsBone Dense1,360 mgper 4 Softgel(s)DSLD:183377
- Vital NutrientsStrontium (Citrate) 227 mgStrontium Citrate · Strontium (Form: as Strontium Citrate)681 mgper 3 Vegetarian Capsule(s)DSLD:56515
- Vital NutrientsStrontium 227 mgStrontium Citrate681 mgper 3 Vegetarian Capsule(s)DSLD:305165
- Vitamin WorldMega Vita Woman 50+ High PotencyStrontium Citrate · Strontium (Form: as Strontium Citrate)20 mgper 2 Tablet(s)DSLD:3274
- VPXMedivinStrontium Carbonate · Strontium (Form: as Strontium Carbonate)50 mgper 1 Package(s)DSLD:55569
- XtendlifeArthrit-EzeStrontium Citrate · Strontium (Form: as Strontium Citrate)1.3 mgper 6 Tablet(s)DSLD:17012
- XtendlifeBone-ProtecStrontium Citrate · Strontium (Form: as Strontium Citrate)1.3 mgper 3 Capsule(s)DSLD:17013
- XtendlifeBone-SupportStrontium Citrate1.2 mgper 3 Capsule(s)DSLD:283344
- XtendlifeBone-SupportStrontium Citrate1.2 mgper 3 Capsule(s)DSLD:318011
- YoungevityBeyond Osteo-fx Tropical VanillaStrontium Chloride · Strontium (Form: from Strontium Chloride)500 mcgper 12 Gram(s)DSLD:277503
- YoungevityBeyond Osteo-fx Tropical Vanilla FlavorStrontium Chloride · Strontium (Form: from Strontium Chloride)500 mcgper 11.9 Gram(s)DSLD:209179
- ZahlerPowerCal 1000 mgStrontium Citrate650 mgper 4 Tablet(s)DSLD:33331
Label record: NIH Office of Dietary Supplements · CC0
Papers screened
89 papers
- Compound
- strontium(2+)
- Screened
- 89
- Admitted
- 4
- Discarded
- 44
- Not read
- 41
Produced a finding4 papers
- PMID:170542532026-10-23
- PMID:194369412026-10-23
- PMID:221245752026-10-23
- PMID:231172452026-10-23
Discarded: the wrong intervention37 papers
- PMID:10541760cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:11502480cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:11683526cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:12699291cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:12730741cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:12730769cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:14555675cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:14749454cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:14969403cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:15106819cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:15537445cited by PMID:19436941; not about the subject it would be filed under2026-10-24
- PMID:15728210cited by PMID:19436941; not about the subject it would be filed under2026-10-24
and 25 more.
Discarded: an endpoint this vocabulary does not hold4 papers
- PMID:22283848no claim extracted — no_outcome_node — measured: QTc interval change (individually heart-rate-corrected, QTcI) from ECG, time-matched difference versus placebo, thorough QT study | QTc interval change, individually heart-rate-corrected QT(c)I on ECG, time-matched versus placebo2026-10-23
- PMID:27434595no claim extracted — endpoint_near_miss — measured: clinical progression-free survival defined as time to pain progression, skeletal-related event or death (not radiological or disease progression), Cox hazard ratio | clinical progression-free survival defined as time to pain progression, skeletal-related event or death, Cox regression2026-10-23
- PMID:29138499no claim extracted — no_outcome_node — measured: bone-to-implant contact percentage around implants, histomorphometry | bone-to-implant contact percentage, histomorphometry2026-10-23
- PMID:33909659no claim extracted — endpoint_near_miss — measured: spontaneous post-bleaching tooth sensitivity, self-reported daily on a 4-point (0-3) modified VAS, no tactile or air-blast stimulus | post-bleaching tooth sensitivity on a 4-point (0-3) modified VAS, daily diary2026-10-23
Discarded: no extractable result1 paper
- PMID:25155428no claim extracted — quote_not_self_supporting2026-10-23
Discarded: another reason, stated per paper1 paper
- PMID:33755674no claim extracted — cause not determined — DOSED: Strontium-90 beta-ray skin applicator brachytherapy, 15-20 Gy total, Methods; a radioisotope radiation source, not strontium(2+) ingested or applied as a compound (one pass only) — measured: keloid recurrence rate at one year, Vancouver Scar Scale with Doppler ultrasound thickness criterion2026-10-23
Discarded: the wrong population1 paper
- PMID:25888851no claim extracted — result_is_subgroup_only2026-10-23
Not read yet41 papers
- PMID:168560922026-10-12
- PMID:172806222026-10-12
- PMID:194644012026-10-12
- PMID:195979102026-10-12
- PMID:198130432026-10-12
- PMID:200262652026-10-12
- PMID:200820662026-10-12
- PMID:205123362026-10-12
- PMID:205337642026-10-12
- PMID:207268142026-10-12
- PMID:208170532026-10-12
- PMID:208722152026-10-12
and 29 more.
Measured, not recorded
- Compound
- strontium(2+)
- Endpoints measured
- 366 endpoints
- Recorded as a finding
- No
Show what was measured
bone mineral density, all sites
increases
An increase in BMD was shown at all BMD sites after two to three years in both populations
PMID:17054253 · one of two readings recorded this
diarrhoea risk with 2 g strontium ranelate (adverse event)
increases
Not recorded as a finding: no node for diarrhoea incidence as an adverse event; diarrhoea-duration node measures time to resolution, a different construct; no estimate stated
An increased risk of diarrhea with 2 g of strontium ranelate was found; however, adverse events did not affect the risk of discontinuing treatment nor did it increase the risk of serious side effects, gastritis or death.
PMID:17054253 · one of two readings recorded this
diarrhoea risk with 2 g strontium ranelate daily, adverse event
increases
Not recorded as a finding: No outcome node for diarrhoea incidence; the sentence gives no estimate.
An increased risk of diarrhea with 2 g of strontium ranelate was found; however, adverse events did not affect the risk of discontinuing treatment nor did it increase the risk of serious side effects, gastritis or death.
PMID:17054253 · one of two readings recorded this
discontinuation of treatment due to adverse events
no effect
adverse events leading to study withdrawal were not significantly increased with taking 2 g of strontium ranelate daily
PMID:17054253 · one of two readings recorded this
non-vertebral fractures
decreases
a 14% reduction in non-vertebral fractures (RR 0.86, 95% CI 0.75, 0.98)
PMID:17054253 · one of two readings recorded this
vertebral fractures and BMD, dose response
increases
Lower doses of strontium ranelate were superior to placebo and the highest dose demonstrated the greatest reduction in vertebral fractures and increase in BMD
PMID:17054253 · one of two readings recorded this
vertebral fractures
decreases
A 37% reduction in vertebral fractures (RR 0.63, 95% CI 0.56, 0.71)
PMID:17054253 · one of two readings recorded this
vertebral fracture incidence
Incidence (%) | 14.9 | 21.1 | 14.3 | 23.7 | 16.4 | 26.5
PMID:19436941 · one of two readings recorded this
vertebral fracture incidence
Incidence (%) | 14.9 | 21.1 | 14.3 | 23.7 | 16.4 | 26.5
PMID:19436941 · one of two readings recorded this
vertebral fracture incidence
Incidence (%) | 14.9 | 21.1 | 14.3 | 23.7 | 16.4 | 26.5
PMID:19436941 · one of two readings recorded this
vertebral fracture incidence
Incidence (%) | 13.8 | 21.2 | 16.9 | 24.1 | 14.7 | 26.3
PMID:19436941 · one of two readings recorded this
vertebral fracture incidence
Incidence (%) | 13.8 | 21.2 | 16.9 | 24.1 | 14.7 | 26.3
PMID:19436941 · one of two readings recorded this
vertebral fracture incidence
Incidence (%) | 13.8 | 21.2 | 16.9 | 24.1 | 14.7 | 26.3
PMID:19436941 · one of two readings recorded this
absolute risk reduction, vertebral fracture
Absolute risk reduction (%) | 6.2 | 9.4 | 10.2
PMID:19436941 · one of two readings recorded this
absolute risk reduction, vertebral fracture
Absolute risk reduction (%) | 6.2 | 9.4 | 10.2
PMID:19436941 · one of two readings recorded this
absolute risk reduction, vertebral fracture
Absolute risk reduction (%) | 6.2 | 9.4 | 10.2
PMID:19436941 · one of two readings recorded this
absolute risk reduction, vertebral fracture
Absolute risk reduction (%) | 7.4 | 7.2 | 11.6
PMID:19436941 · one of two readings recorded this
absolute risk reduction, vertebral fracture
Absolute risk reduction (%) | 7.4 | 7.2 | 11.6
PMID:19436941 · one of two readings recorded this
absolute risk reduction, vertebral fracture
Absolute risk reduction (%) | 7.4 | 7.2 | 11.6
PMID:19436941 · one of two readings recorded this
lumbar BMD change from baseline
increases
The increase in lumbar BMD with strontium ranelate, relative to baseline, at 3 years was 12.5%, 14.6% and 16.5% in b-ALP tertile 1, 2 and 3, respectively
PMID:19436941 · one of two readings recorded this
lumbar BMD change from baseline
increases
The increase in lumbar BMD with strontium ranelate, relative to baseline, at 3 years was 12.5%, 14.6% and 16.5% in b-ALP tertile 1, 2 and 3, respectively
PMID:19436941 · one of two readings recorded this
lumbar BMD change from baseline
increases
The increase in lumbar BMD with strontium ranelate, relative to baseline, at 3 years was 12.5%, 14.6% and 16.5% in b-ALP tertile 1, 2 and 3, respectively
PMID:19436941 · one of two readings recorded this
lumbar BMD change from baseline
increases
12.6%, 13.9% and 16.9% in sCTX tertile 1, 2, and 3, respectively
PMID:19436941 · one of two readings recorded this
lumbar BMD change from baseline
increases
12.6%, 13.9% and 16.9% in sCTX tertile 1, 2, and 3, respectively
PMID:19436941 · one of two readings recorded this
lumbar BMD change from baseline
increases
12.6%, 13.9% and 16.9% in sCTX tertile 1, 2, and 3, respectively
PMID:19436941 · one of two readings recorded this
lumbar spine BMD by DXA (Hologic), percent change from baseline at 3 years, by tertile of baseline bone turnover
increases
Not recorded as a finding: The sentence naming the between-group contrast does not name lumbar BMD, and the percent-increase sentence is relative to baseline within the strontium ranelate arm; only tertile-stratified results are given.
Lumbar BMD increased progressively during the 3-year analysis period in patients treated with strontium ranelate, but remained virtually unchanged in placebo-treated patients.
PMID:19436941 · one of two readings recorded this
new vertebral fracture incidence, placebo highest vs lowest tertile
increases, p = 0.01
26.5% vs 21.1% in b-ALP tertiles 3 and 1, p = 0.010
PMID:19436941 · one of two readings recorded this
new vertebral fracture incidence, placebo highest vs lowest tertile
increases, p = 0.043
26.3% vs 21.2% in sCTX tertiles 3 and 1, p = 0.043
PMID:19436941 · one of two readings recorded this
new vertebral fracture relative risk, placebo high vs low bone turnover
increases
by 32% when considering b-ALP (RR = 1.32, 95% CI [1.06; 1.62])
PMID:19436941 · one of two readings recorded this
new vertebral fracture relative risk, placebo high vs low bone turnover
increases, p = 0.012
RR = 1.47, 95% CI [1.08; 1.97], p = 0.012
PMID:19436941 · one of two readings recorded this
new vertebral fracture relative risk, placebo high vs low bone turnover
increases
24% when considering sCTX (RR = 1.24, 95% CI [1.00; 1.54])
PMID:19436941 · one of two readings recorded this
new vertebral fracture, SR vs placebo, all patients
decreases, p = 0.001
RR = 0.60, 95% CI [0.53–0.70], p < 0.001
PMID:19436941 · one of two readings recorded this
new vertebral fracture, SR vs placebo
decreases, p = 0.001
the relative risk reduction with strontium ranelate was 49% (RR = 0.51, 95% CI [0.37; 0.70], p <0.001)
PMID:19436941 · one of two readings recorded this
new vertebral fracture, SR vs placebo
decreases, p = 0.023
RR reduction of 33% compared to placebo (RR = 0.67, 95% CI [0.47; 0.95], p = 0.023
PMID:19436941 · one of two readings recorded this
number needed to treat, vertebral fracture
NNT | 17 | 11 | 10
PMID:19436941 · one of two readings recorded this
number needed to treat, vertebral fracture
NNT | 17 | 11 | 10
PMID:19436941 · one of two readings recorded this
number needed to treat, vertebral fracture
NNT | 17 | 11 | 10
PMID:19436941 · one of two readings recorded this
number needed to treat, vertebral fracture
NNT | 14 | 14 | 9
PMID:19436941 · one of two readings recorded this
number needed to treat, vertebral fracture
NNT | 14 | 14 | 9
PMID:19436941 · one of two readings recorded this
number needed to treat, vertebral fracture
NNT | 14 | 14 | 9
PMID:19436941 · one of two readings recorded this
treatment effect heterogeneity across tertiles, new vertebral fracture
no effect, p = 0.513
interaction test p = 0.513 for b-ALP tertiles
PMID:19436941 · one of two readings recorded this
treatment effect heterogeneity across tertiles, new vertebral fracture
no effect, p = 0.29
p = 0.290 for sCTX tertiles
PMID:19436941 · one of two readings recorded this
treatment effect heterogeneity across tertiles, new vertebral fracture
no effect, p = 0.254
interaction test p = 0.254
PMID:19436941 · one of two readings recorded this
vertebral fracture events
Eventsa | 114 | 155 | 107 | 175 | 115 | 203
PMID:19436941 · one of two readings recorded this
vertebral fracture events
Eventsa | 114 | 155 | 107 | 175 | 115 | 203
PMID:19436941 · one of two readings recorded this
vertebral fracture events
Eventsa | 114 | 155 | 107 | 175 | 115 | 203
PMID:19436941 · one of two readings recorded this
vertebral fracture events
Eventsa | 105 | 153 | 122 | 181 | 103 | 195
PMID:19436941 · one of two readings recorded this
vertebral fracture events
Eventsa | 105 | 153 | 122 | 181 | 103 | 195
PMID:19436941 · one of two readings recorded this
vertebral fracture events
Eventsa | 105 | 153 | 122 | 181 | 103 | 195
PMID:19436941 · one of two readings recorded this
vertebral fracture relative risk
decreases
Relative risk [95% CI] | 0.69 [0.54; 0.88] | 0.58 [0.46; 0.74] | 0.58 [0.46; 0.73]
PMID:19436941 · one of two readings recorded this
vertebral fracture relative risk
decreases
Relative risk [95% CI] | 0.69 [0.54; 0.88] | 0.58 [0.46; 0.74] | 0.58 [0.46; 0.73]
PMID:19436941 · one of two readings recorded this
vertebral fracture relative risk
decreases
Relative risk [95% CI] | 0.69 [0.54; 0.88] | 0.58 [0.46; 0.74] | 0.58 [0.46; 0.73]
PMID:19436941 · one of two readings recorded this
vertebral fracture relative risk
decreases
Relative risk [95% CI] | 0.63 [0.49; 0.81] | 0.68 [0.54; 0.85] | 0.53 [0.42; 0.67]
PMID:19436941 · one of two readings recorded this
vertebral fracture relative risk
decreases
Relative risk [95% CI] | 0.63 [0.49; 0.81] | 0.68 [0.54; 0.85] | 0.53 [0.42; 0.67]
PMID:19436941 · one of two readings recorded this
vertebral fracture relative risk
decreases
Relative risk [95% CI] | 0.63 [0.49; 0.81] | 0.68 [0.54; 0.85] | 0.53 [0.42; 0.67]
PMID:19436941 · one of two readings recorded this
vertebral fracture RR reduction within tertiles of baseline b-ALP and sCTX (subgroups)
decreases
Not recorded as a finding: subgroup stratum results; whole-population estimate recorded instead
The magnitudes of the treatment effects were not significantly different between tertiles (interaction test p = 0.513 for b-ALP tertiles, p = 0.290 for sCTX tertiles).
PMID:19436941 · one of two readings recorded this
vertebral fracture, SR vs placebo p value
decreases, p = 0.003
p value | 0.003 | <0.001 | <0.001
PMID:19436941 · one of two readings recorded this
vertebral fracture, SR vs placebo p value
decreases, p = 0.001
p value | 0.003 | <0.001 | <0.001
PMID:19436941 · one of two readings recorded this
vertebral fracture, SR vs placebo p value
decreases, p = 0.001
p value | 0.003 | <0.001 | <0.001
PMID:19436941 · one of two readings recorded this
vertebral fracture, SR vs placebo p value
decreases, p = 0.001
p value | <0.001 | <0.001 | <0.001
PMID:19436941 · one of two readings recorded this
vertebral fracture, SR vs placebo p value
decreases, p = 0.001
p value | <0.001 | <0.001 | <0.001
PMID:19436941 · one of two readings recorded this
vertebral fracture, SR vs placebo p value
decreases, p = 0.001
p value | <0.001 | <0.001 | <0.001
PMID:19436941 · one of two readings recorded this
association of femoral neck BMD change with vertebral fracture incidence, years 9 to 10
p = 0.03
the change in femoral neck BMD from years 9 to 10 was significantly associated with vertebral fractures incidence during the same period of time (P = 0.03)
PMID:22124575 · one of two readings recorded this
compliance with strontium ranelate
The mean persistence with strontium ranelate in the 10-year population was 117.8 ± 6.1 months (i.e. 9 years and 9 months); the mean compliance was 89.4 ± 12.6%
PMID:22124575 · one of two readings recorded this
cumulative incidence of any osteoporotic fracture, years 6 to 10 vs years 0 to 5
no effect, p = 0.734
The cumulative incidence of new fracture in the 10-year population in years 6 to 10 was similar to the cumulative incidence in years 0 to 5 (vertebral fracture: 20.6 ± 3.0% versus 18.5 ± 2.6%, respectively, P = 1.00; non-vertebral fracture: 13.7 ± 2.3% versus 12.9 ± 2.2%, P = 0.672; and any osteoporotic fracture: 30.3 ± 3.1% versus 27.5 ± 2.9%, P = 0.734)
PMID:22124575 · one of two readings recorded this
cumulative incidence of new non-vertebral fracture, years 6 to 10 vs years 0 to 5
no effect, p = 0.672
The cumulative incidence of new fracture in the 10-year population in years 6 to 10 was similar to the cumulative incidence in years 0 to 5 (vertebral fracture: 20.6 ± 3.0% versus 18.5 ± 2.6%, respectively, P = 1.00; non-vertebral fracture: 13.7 ± 2.3% versus 12.9 ± 2.2%, P = 0.672; and any osteoporotic fracture: 30.3 ± 3.1% versus 27.5 ± 2.9%, P = 0.734)
PMID:22124575 · one of two readings recorded this
cumulative incidence of new osteoporotic fracture vs FRAX-matched placebo
decreases, p = 0.012
Similarly, the 10-year population had significantly lower rates of nonvertebral fracture and new osteoporotic fracture in years 6 to 10 than the FRAX®-matched placebo population over 5 years (nonvertebral fracture: 13.7 ± 2.3% versus 20.2 ± 2.2%, respectively, RRR 38%, P = 0.023; new osteoporotic fracture: 30.3 ± 3.1% versus 39.2 ± 2.5%, RRR 30%, P = 0.012)
PMID:22124575 · one of two readings recorded this
cumulative incidence of new vertebral fracture vs FRAX-matched placebo
decreases, p = 0.016
The cumulative incidence of new vertebral fractures in the 10-year population in years 6 to 10 was significantly lower than that observed over 5 years in the FRAX®-matched placebo population (20.6 ± 3.0% versus 28.2 ± 2.4%, respectively; relative reduction in risk [RRR] 35%, P = 0.016)
PMID:22124575 · one of two readings recorded this
cumulative incidence of new vertebral fracture, years 6 to 10 vs years 0 to 5
no effect, p = 1
The cumulative incidence of new fracture in the 10-year population in years 6 to 10 was similar to the cumulative incidence in years 0 to 5 (vertebral fracture: 20.6 ± 3.0% versus 18.5 ± 2.6%, respectively, P = 1.00; non-vertebral fracture: 13.7 ± 2.3% versus 12.9 ± 2.2%, P = 0.672; and any osteoporotic fracture: 30.3 ± 3.1% versus 27.5 ± 2.9%, P = 0.734)
PMID:22124575 · one of two readings recorded this
cumulative incidence of nonvertebral fracture vs FRAX-matched placebo
decreases, p = 0.023
Similarly, the 10-year population had significantly lower rates of nonvertebral fracture and new osteoporotic fracture in years 6 to 10 than the FRAX®-matched placebo population over 5 years (nonvertebral fracture: 13.7 ± 2.3% versus 20.2 ± 2.2%, respectively, RRR 38%, P = 0.023; new osteoporotic fracture: 30.3 ± 3.1% versus 39.2 ± 2.5%, RRR 30%, P = 0.012)
PMID:22124575 · one of two readings recorded this
femoral neck BMD change, years 9 to 10, by new vertebral fracture status
Women with new vertebral fractures from years 9 to 10 experienced a simultaneous decrease of 2.4 ± 4.7% in femoral neck BMD, compared with an increase of 1.5 ± 8.3% in women without new vertebral fracture
PMID:22124575 · one of two readings recorded this
femoral neck BMD mean change, baseline to year 10
increases, n = 147
Baseline to year 10 | 147 | 0.060 ± 0.066*** | 10.7 ± 12.1***
PMID:22124575 · one of two readings recorded this
femoral neck BMD mean change, years 0-5
increases, n = 225
Years 0–5 | 225 | 0.050 ± 0.044*** | 8.8 ± 8.0***
PMID:22124575 · one of two readings recorded this
femoral neck BMD mean change, years 6–10
n = 130
Years 6–10 | 130 | 0.010 ± 0.056* | 1.8 ± 9.1*
PMID:22124575 · one of two readings recorded this
femoral neck BMD mean relative change, baseline to year 10
increases, n = 147
Baseline to year 10 | 147 | 0.060 ± 0.066*** | 10.7 ± 12.1***
PMID:22124575 · one of two readings recorded this
femoral neck BMD mean relative change, years 0-5
increases, n = 225
Years 0–5 | 225 | 0.050 ± 0.044*** | 8.8 ± 8.0***
PMID:22124575 · one of two readings recorded this
femoral neck BMD mean relative change, years 6–10
n = 130
Years 6–10 | 130 | 0.010 ± 0.056* | 1.8 ± 9.1*
PMID:22124575 · one of two readings recorded this
lumbar spine BMD by DXA (Hologic), mean relative change from baseline over 10 years, single arm
increases, 34.5 ± 20.2% relative change from baseline to year 10
Not recorded as a finding: Within-arm change from baseline in an open-label single-arm extension; there is no between-arm contrast for BMD.
Over the 10-year period, lumbar BMD increased continuously with a mean relative change from baseline of 34.5 ± 20.2% (Table 3) in the 10-year population treated with strontium ranelate.
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD mean change, baseline to year 10
increases, n = 155
Baseline to year 10 | 155 | 0.253 ± 0.151*** | 34.5 ± 20.2***
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD mean change, years 0-5
increases, n = 223
Years 0–5 | 223 | 0.179 ± 0.105*** | 23.9 ± 13.9***
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD mean change, years 6-10
increases, n = 146
Years 6-10 | 146 | 0.070 ± 0.115** | 7.9 ± 12.6**
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD mean relative change, baseline to year 10
increases, n = 155
Baseline to year 10 | 155 | 0.253 ± 0.151*** | 34.5 ± 20.2***
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD mean relative change, years 0-5
increases, n = 223
Years 0–5 | 223 | 0.179 ± 0.105*** | 23.9 ± 13.9***
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD mean relative change, years 6-10
increases, n = 146
Years 6-10 | 146 | 0.070 ± 0.115** | 7.9 ± 12.6**
PMID:22124575 · one of two readings recorded this
lumbar spine L2-L4 BMD relative change from baseline over 10 years, DXA
increases, 34.5 ± 20.2% mean relative change from baseline at year 10
Not recorded as a finding: within-arm change over time with no control arm (lumbar-spine-bmd node; no between-group contrast)
Over the 10-year period, lumbar BMD increased continuously with a mean relative change from baseline of 34.5 ± 20.2% (Table 3) in the 10-year population treated with strontium ranelate.
PMID:22124575 · one of two readings recorded this
new vertebral fracture risk per 1% increase in femoral neck BMD, years 9 to 10
decreases
Each 1% increase in femoral neck BMD was associated with a 15% (95% adjusted confidence interval [CI] 2–26%) decrease in risk for new vertebral fracture
PMID:22124575 · one of two readings recorded this
new vertebral fracture risk per 1% increase in total hip BMD, years 9 to 10
no effect, p = 0.16
The same trend was observed for total hip BMD (7%; 95% CI 3–17%), but did not reach statistical significance (P = 0.16)
PMID:22124575 · one of two readings recorded this
persistence with strontium ranelate
The mean persistence with strontium ranelate in the 10-year population was 117.8 ± 6.1 months (i.e. 9 years and 9 months); the mean compliance was 89.4 ± 12.6%
PMID:22124575 · one of two readings recorded this
total hip BMD mean change, baseline to year 10
increases, n = 147
Baseline to year 10 | 147 | 0.077 ± 0.084*** | 11.7 ± 13.6***
PMID:22124575 · one of two readings recorded this
total hip BMD mean change, years 0-5
increases, n = 225
Years 0–5 | 225 | 0.080 ± 0.056*** | 12.1 ± 11.2***
PMID:22124575 · one of two readings recorded this
total hip BMD mean change, years 6–10
n = 130
Years 6–10 | 130 | 0.000 ± 0.067 | 0.04 ± 8.9
PMID:22124575 · one of two readings recorded this
total hip BMD mean relative change, baseline to year 10
increases, n = 147
Baseline to year 10 | 147 | 0.077 ± 0.084*** | 11.7 ± 13.6***
PMID:22124575 · one of two readings recorded this
total hip BMD mean relative change, years 0-5
increases, n = 225
Years 0–5 | 225 | 0.080 ± 0.056*** | 12.1 ± 11.2***
PMID:22124575 · one of two readings recorded this
total hip BMD mean relative change, years 6–10
n = 130
Years 6–10 | 130 | 0.000 ± 0.067 | 0.04 ± 8.9
PMID:22124575 · one of two readings recorded this
largest time-matched mean QTc interval change from baseline versus placebo (individual heart-rate correction, QTcI), automated ECG with manual over-reading, in healthy volunteers given strontium ranelate 4 g/day for 15 days
no effect
Not recorded as a finding: this platform holds no node for the endpoint
The findings of this study demonstrate that the administration of supratherapeutic repeated oral doses of strontium ranelate (4 g day⁻¹ for 15 days) does not lead to a prolongation of the QT/QT(c) interval above the threshold of regulatory concern.
PMID:22283848 · one of two readings recorded this
largest time-matched QT(c)I difference versus placebo
For strontium ranelate (4 g day⁻¹) the largest time-matched difference in QT(c) I compared with placebo was observed at 1 h post dose (mean [90% CI] 7.54 [5.17, 9.90] ms)
PMID:22283848 · one of two readings recorded this
largest time-matched QT(c)I difference versus placebo
increases
The largest time-matched difference in QT(c) I (individual QT correction for heart rate) between moxifloxacin 400 mg and placebo was observed at 2 h post dose (mean [95% CI] 10.62 [7.90, 13.35] ms)
PMID:22283848 · one of two readings recorded this
QT/QT(c) interval prolongation above threshold of regulatory concern
no effect
The findings of this study demonstrate that the administration of supratherapeutic repeated oral doses of strontium ranelate (4 g day⁻¹ for 15 days) does not lead to a prolongation of the QT/QT(c) interval above the threshold of regulatory concern
PMID:22283848 · one of two readings recorded this
subjects with QT(c) greater than 480 ms
no effect
No subject had a QT(c) greater than 480 ms during the study
PMID:22283848 · one of two readings recorded this
creatine phosphokinase change from baseline
creatine phosphokinase, which increased from baseline with treatment (11.7±85.6 and 20.7±104.4 IU/l with 1 and 2 g/day, respectively), but not placebo (−0.4±68.1 IU/l)
PMID:23117245 · one of two readings recorded this
global knee pain (VAS) change
no effect, p = 0.884
Global knee pain (VAS), (/100 mm) | −22.9 (29.0) | −0.24 (1.64) (−3.45 to 2.97) | 0.884 | −28.5 (28.3) | −3.01 (1.60) (−6.20 to 0.19) | 0.065 | −24.2 (29.2)
PMID:23117245 · one of two readings recorded this
global knee pain (VAS) change
no effect, p = 0.065
Global knee pain (VAS), (/100 mm) | −22.9 (29.0) | −0.24 (1.64) (−3.45 to 2.97) | 0.884 | −28.5 (28.3) | −3.01 (1.60) (−6.20 to 0.19) | 0.065 | −24.2 (29.2)
PMID:23117245 · one of two readings recorded this
joint space width change, 1 g/day vs 2 g/day
no effect, p = 0.601
The change in JSW from baseline was significantly different from placebo in both treatment groups at 12, 24 and 36 months, with no difference between the dosages at any time (p=0.601 at 12 months, p=0.149 at 24 months and p=0.311 at 36 months)
PMID:23117245 · one of two readings recorded this
joint space width change, 1 g/day vs 2 g/day
no effect, p = 0.149
The change in JSW from baseline was significantly different from placebo in both treatment groups at 12, 24 and 36 months, with no difference between the dosages at any time (p=0.601 at 12 months, p=0.149 at 24 months and p=0.311 at 36 months)
PMID:23117245 · one of two readings recorded this
joint space width change, 1 g/day vs 2 g/day
no effect, p = 0.311
The change in JSW from baseline was significantly different from placebo in both treatment groups at 12, 24 and 36 months, with no difference between the dosages at any time (p=0.601 at 12 months, p=0.149 at 24 months and p=0.311 at 36 months)
PMID:23117245 · one of two readings recorded this
joint space width change (medial tibiofemoral compartment)
increases, p = 0.001
Joint space width (mm) | −0.23 (0.56) | 0.14 (0.04) (0.05 to 0.23) | <0.001 | −0.27 (0.63) | 0.10 (0.04) (0.02 to 0.19) | 0.018 | −0.37 (0.59)
PMID:23117245 · one of two readings recorded this
joint space width change (medial tibiofemoral compartment)
increases, p = 0.018
Joint space width (mm) | −0.23 (0.56) | 0.14 (0.04) (0.05 to 0.23) | <0.001 | −0.27 (0.63) | 0.10 (0.04) (0.02 to 0.19) | 0.018 | −0.37 (0.59)
PMID:23117245 · one of two readings recorded this
radioclinical progression
decreases, p = 0.049
Radioclinical progression† | 32 (8%) | −3.94 (1.98) (−7.83 to −0.05) | 0.049 | 28 (7%) | −5.12 (1.91) (−8.86 to −1.37) | 0.008 | 53 (12%)
PMID:23117245 · one of two readings recorded this
radioclinical progression
decreases, p = 0.008
Radioclinical progression† | 32 (8%) | −3.94 (1.98) (−7.83 to −0.05) | 0.049 | 28 (7%) | −5.12 (1.91) (−8.86 to −1.37) | 0.008 | 53 (12%)
PMID:23117245 · one of two readings recorded this
radiographic joint space narrowing (minimal medial tibiofemoral JSW, mm, computer-assisted) over 3 years, primary endpoint
decreases
Not recorded as a finding: radiographic-joint-space-narrowing node requires standardised weight-bearing knee radiographs; the paper states a fixed-flexion posteroanterior view with positioning frame and never says weight-bearing (instrument not stated)
Treatment with strontium ranelate was associated with significantly attenuated JSN versus placebo, with −0.23±0.56 mm for 1 g/day and −0.27±0.63 mm for 2 g/day from baseline to end (table 2).
PMID:23117245 · one of two readings recorded this
radiological progression, joint space narrowing of 0.5 mm or more over 3 years (proportion of progressors)
decreases
Not recorded as a finding: Node incident-knee-oa-mjsn-progression defines progression as at least 1 mm in the medial compartment; this paper uses a 0.5 mm threshold, a different definition.
There were significantly fewer radiological and radioclinical progressors with strontium ranelate 1 and 2 g/day (table 2).
PMID:23117245 · one of two readings recorded this
radiological progression (JSN ≥0.5 mm)
decreases, p = 0.001
Radiological progression* | 99 (22%) | −10.80 (2.9) (−16.54 to −5.06) | <0.001 | 116 (26%) | −7.50 (3.0) (−13.34 to −1.66) | 0.012 | 156 (33%)
PMID:23117245 · one of two readings recorded this
radiological progression (JSN ≥0.5 mm)
decreases, p = 0.012
Radiological progression* | 99 (22%) | −10.80 (2.9) (−16.54 to −5.06) | <0.001 | 116 (26%) | −7.50 (3.0) (−13.34 to −1.66) | 0.012 | 156 (33%)
PMID:23117245 · one of two readings recorded this
radiological progression (JSN of 0.5 mm or more over 3 years) and radioclinical progression, proportion of progressors
decreases
Not recorded as a finding: no node for a 0.5 mm JSN progressor proportion; incident-knee-oa-mjsn-progression requires 1 mm in the medial compartment on weight-bearing films
There were significantly fewer radiological and radioclinical progressors with strontium ranelate 1 and 2 g/day (table 2).
PMID:23117245 · one of two readings recorded this
treatment compliance
Mean compliance was 93.3±9.3% (ITT population)
PMID:23117245 · one of two readings recorded this
urinary CTX-II relative change, ELISA
decreases, between-group difference significant versus placebo for both doses
Not recorded as a finding: sentence never names strontium ranelate (agentless 'between-group difference'), so it does not support the claim on its own
Urinary CTX-II decreased in all groups, and the between-group difference in the relative change was significant for both dosages versus placebo (p=0.003 for 1 g/day and p=0.021 for 2 g/day).
PMID:23117245 · one of two readings recorded this
urinary CTX-II relative change
decreases, p = 0.003
Urinary CTX-II decreased in all groups, and the between-group difference in the relative change was significant for both dosages versus placebo (p=0.003 for 1 g/day and p=0.021 for 2 g/day)
PMID:23117245 · one of two readings recorded this
urinary CTX-II relative change
decreases, p = 0.021
Urinary CTX-II decreased in all groups, and the between-group difference in the relative change was significant for both dosages versus placebo (p=0.003 for 1 g/day and p=0.021 for 2 g/day)
PMID:23117245 · one of two readings recorded this
WOMAC pain subscore change
no effect, p = 0.969
WOMAC pain subscore (/100 mm) | −14.6 (22.6) | 0.1 (1.3) (−2.6 to 2.7) | 0.969 | −19.1 (23.7) | −3.0 (1.3) (−5.6 to −0.3) | 0.028 | −14.7 (23.5)
PMID:23117245 · one of two readings recorded this
WOMAC pain subscore change
decreases, p = 0.028
WOMAC pain subscore (/100 mm) | −14.6 (22.6) | 0.1 (1.3) (−2.6 to 2.7) | 0.969 | −19.1 (23.7) | −3.0 (1.3) (−5.6 to −0.3) | 0.028 | −14.7 (23.5)
PMID:23117245 · one of two readings recorded this
WOMAC pain subscore change
decreases, p = 0.029
The reduction in total WOMAC score and pain subscore was numerically greater with treatment than placebo at every visit, with a significant between-group difference for pain subscore at 36 months (p=0.029 for 2 g/day)
PMID:23117245 · one of two readings recorded this
WOMAC physical function subscore change
no effect, p = 0.772
WOMAC physical function subscore (/100 mm) | −12.2 (21.1) | −0.4 (1.3) (−3.0 to 2.2) | 0.772 | −15.0 (22.2) | −2.2 (1.3) (−4.7 to 0.4) | 0.099 | −11.7 (23.2)
PMID:23117245 · one of two readings recorded this
WOMAC physical function subscore change
no effect, p = 0.099
WOMAC physical function subscore (/100 mm) | −12.2 (21.1) | −0.4 (1.3) (−3.0 to 2.2) | 0.772 | −15.0 (22.2) | −2.2 (1.3) (−4.7 to 0.4) | 0.099 | −11.7 (23.2)
PMID:23117245 · one of two readings recorded this
WOMAC stiffness subscore change
no effect, p = 0.523
WOMAC stiffness subscore (/100 mm) | −15.6 (26.9) | −1.0 (1.6) (−4.1 to 2.1) | 0.523 | −18.3 (28.0) | −2.5 (1.6) (−5.6 to 0.6) | 0.120 | −14.0 (29.4)
PMID:23117245 · one of two readings recorded this
WOMAC stiffness subscore change
no effect, p = 0.12
WOMAC stiffness subscore (/100 mm) | −15.6 (26.9) | −1.0 (1.6) (−4.1 to 2.1) | 0.523 | −18.3 (28.0) | −2.5 (1.6) (−5.6 to 0.6) | 0.120 | −14.0 (29.4)
PMID:23117245 · one of two readings recorded this
WOMAC total score, 0 to 300 mm, 2 g/day versus placebo
decreases, p = 0.045
Not recorded as a finding: No outcome node for WOMAC total score; only the pain, stiffness and function subscales have nodes.
Treatment with strontium ranelate 2 g/day was associated with significantly lower WOMAC total score (p=0.045) and pain subscore (p=0.028), and a trend toward lower physical function subscore (p=0.099) and global knee pain (p=0.065) (table 2).
PMID:23117245 · one of two readings recorded this
WOMAC total score change
no effect, p = 0.749
WOMAC total score (/300 mm) | −41.8 (62.3) | −1.3 (4.0) (−9.0 to 6.5) | 0.749 | −51.9 (66.1) | −8.0 (4.0) (−15.7 to −0.2) | 0.045 | −40.7 (69.1)
PMID:23117245 · one of two readings recorded this
WOMAC total score change
decreases, p = 0.045
WOMAC total score (/300 mm) | −41.8 (62.3) | −1.3 (4.0) (−9.0 to 6.5) | 0.749 | −51.9 (66.1) | −8.0 (4.0) (−15.7 to −0.2) | 0.045 | −40.7 (69.1)
PMID:23117245 · one of two readings recorded this
deaths
Of 79 randomized patients, 50 (63.3%) died: 24 (60.0%) of 40 patients in the control arm and 26 (66.7%) of 39 patients in the Sr-89 treatment arm
PMID:25155428 · one of two readings recorded this
disease progression events
Of the 79 randomized patients, 56 (70.9%) had disease progression: 28 (70.0%) of 40 patients in the control arm and 28 (71.8%) of 39 patients in the Sr-89 treatment arm
PMID:25155428 · one of two readings recorded this
median nadir PSA
The median nadir PSA levels for patients with ≤6 bone metastases who received and did not receive Sr-89 were 0.1 [range: <0.1–30] and 0.1 [range: <0.1–23.8], respectively, and for those patients with >6 bone metastases, 1.0 [range: <0.1–29] and 0.9 [range: <0.1–87.5], respectively
PMID:25155428 · one of two readings recorded this
median overall survival
Median Ross were 53.5 months (95% CI: 38.0, not attained) in the control arm and 47.4 months (95% CI: 35.9, 87.3) in the treatment arm
PMID:25155428 · one of two readings recorded this
median progression-free survival
Median PFS was 18.5 months (95% CI: [9.7, 49.4]) in the control arm compared with 12.9 months (95% CI: (8.9, 72.5)) in the Sr-89 arm
PMID:25155428 · one of two readings recorded this
overall survival, between-arm comparison
no effect, p = 0.97
OS did not differ statistically between the arms (= 0.97)
PMID:25155428 · one of two readings recorded this
progression-free survival, between-arm comparison
no effect, p = 0.86
PFS did not differ statistically between the two arms (= 0.86)
PMID:25155428 · one of two readings recorded this
progression-free survival by number of bone metastases (test of equality over strata)
modulates, p = 0.02
The test of equality over stratum of EOD showed that it was heterogeneous (p=0.02)
PMID:25155428 · one of two readings recorded this
progression-free survival, time from randomization to first disease progression or death, Kaplan-Meier, with one dose of strontium-89 (4 mCi iv) added to androgen deprivation, doxorubicin and zoledronic acid in castrate-sensitive prostate cancer with bone metastases
no effect, p = 0.86
Not recorded as a finding: the supporting sentence never names the compound
PFS did not differ statistically between the two arms (= 0.86).
PMID:25155428 · one of two readings recorded this
progression-free survival (time from randomization to first evidence of disease progression or death), Kaplan-Meier; overall survival
no effect
Not recorded as a finding: the supporting sentence never names the compound
PFS did not differ statistically between the two arms (= 0.86).
PMID:25155428 · one of two readings recorded this
bone mineral density at the lumbar spine (L1-L4) and proximal femora by DEXA (g/cm2) after 6 months of strontium ranelate 2 g/day
increases, BMD increases significantly versus baseline and versus control in both strontium ranelate groups
Not recorded as a finding: the intervention held more than the compound
Increases in BMD were observed at both the lumbar spine (L1–L4) and proximal femora in both strontium ranelate treatment groups (Table 2; Fig. 1).
PMID:25480348 · one of two readings recorded this
collum femoris BMD percent change
increases
% Change (↓ ↑) (mean ± SD) | ↑ 0.06 ± 0.02 | ↑ 3.20 ± 0.46 | ↑ 8.17 ± 1.44
PMID:25480348 · one of two readings recorded this
collum femoris BMD
BMD (g/cm2, mean ± SD) | 0.780 ± 0.01 | 0.781 ± 0.01 | 0.780 ± 0.003 | 0.805 ± 0.01 | 0.799 ± 0.02 | 0.862 ± 0.02
PMID:25480348 · one of two readings recorded this
equilibrium test time
Equilibrium test (s, mean ± SD) | 6.49 ± 2.54 | 6.49 ± 2.45 | 6.68 ± 2.95 | 6.69 ± 2.88 | 6.26 ± 2.35 | 8.88 ± 1.50
PMID:25480348 · one of two readings recorded this
lumbar spine BMD (L1–L4) percent change
increases
% Change (↓ ↑) (mean ± SD) | ↑ 0.24 ± 0.45 | ↑ 4.65 ± 0.56 | ↑ 8.18 ± 0.62
PMID:25480348 · one of two readings recorded this
lumbar spine BMD (L1–L4)
BMD (g/cm2, mean ± SD) | 0.741 ± 0.02 | 0.742 ± 0.01 | 0.746 ± 0.01 | 0.780 ± 0.01 | 0.749 ± 0.01 | 0.810 ± 0.01
PMID:25480348 · one of two readings recorded this
lumbar spine (L1-L4) and proximal femur bone mineral density by DEXA (Lunar Prodigy), g/cm2, after 6 months
increases, BMD increases at lumbar spine and proximal femora in both strontium ranelate groups, significant versus baseline and versus control
Not recorded as a finding: the intervention held more than the compound
Increases in BMD were observed at both the lumbar spine (L1–L4) and proximal femora in both strontium ranelate treatment groups (Table 2; Fig. 1).
PMID:25480348 · one of two readings recorded this
rising from a chair test time
Rising from a chair test (s, mean ± SD) | 16.85 ± 2.31 | 16.81 ± 2.36 | 16.61 ± 2.55 | 16.54 ± 2.55 | 16.83 ± 3.12 | 13.86 ± 2.53
PMID:25480348 · one of two readings recorded this
serum β-CrossLaps reduction from baseline
decreases
Serum levels of β-CrossLaps were reduced compared with baseline in both strontium ranelate groups, by 18.7 % with SrRan and 37.7 % with SrRan + AD3
PMID:25480348 · one of two readings recorded this
serum β-CrossLaps reduction from baseline
decreases
Serum levels of β-CrossLaps were reduced compared with baseline in both strontium ranelate groups, by 18.7 % with SrRan and 37.7 % with SrRan + AD3
PMID:25480348 · one of two readings recorded this
serum β-CrossLaps reduction versus control
decreases, p = 0.0001
After 6 months of therapy, this marker of bone resorption was significantly reduced compared with control in patients receiving SrRan (20.3 %, P = 0.03) and SrRan + AD3 (39.4 %, P < 0.0001)
PMID:25480348 · one of two readings recorded this
serum β-CrossLaps reduction versus control
decreases, p = 0.03
After 6 months of therapy, this marker of bone resorption was significantly reduced compared with control in patients receiving SrRan (20.3 %, P = 0.03) and SrRan + AD3 (39.4 %, P < 0.0001)
PMID:25480348 · one of two readings recorded this
serum β-CrossLaps reduction
decreases, p = 0.008
A significantly greater reduction was also observed in the SrRan + AD3 group compared with SrRan only (24.0 %; P = 0.008)
PMID:25480348 · one of two readings recorded this
serum β-CrossLaps
β-CrossLaps (ng/ml, mean ± SD) | 0.500 ± 0.16 | 0.482 ± 0.16 | 0.481 ± 0.16 | 0.384 ± 0.11 | 0.472 ± 0.04 | 0.292 ± 0.03
PMID:25480348 · one of two readings recorded this
serum PTH reduction
decreases
Reductions in mean PTH values were observed in the SrRan, SrRan + AD3 and control groups: 5.8, 9.3 and 2.3 %, respectively
PMID:25480348 · one of two readings recorded this
serum PTH reduction
decreases
Reductions in mean PTH values were observed in the SrRan, SrRan + AD3 and control groups: 5.8, 9.3 and 2.3 %, respectively
PMID:25480348 · one of two readings recorded this
serum PTH reduction
decreases
Reductions in mean PTH values were observed in the SrRan, SrRan + AD3 and control groups: 5.8, 9.3 and 2.3 %, respectively
PMID:25480348 · one of two readings recorded this
serum PTH
PTH (pg/ml, mean ± SD) | 68.2 ± 14.5 | 66.7 ± 14.5 | 69.4 ± 7.69 | 65.4 ± 8.35 | 71.1 ± 9.53 | 64.6 ± 9.74
PMID:25480348 · one of two readings recorded this
serum TP1NP increase from baseline
increases, p = 0.001
Increases in TP1NP, a marker of bone formation, reached statistical significance in women receiving SrRan or a combination of SrRan + AD3 compared with baseline (35.9 %, P < 0.0001, and 51.4 %, P < 0.001, respectively)
PMID:25480348 · one of two readings recorded this
serum TP1NP increase from baseline
increases, p = 0.0001
Increases in TP1NP, a marker of bone formation, reached statistical significance in women receiving SrRan or a combination of SrRan + AD3 compared with baseline (35.9 %, P < 0.0001, and 51.4 %, P < 0.001, respectively)
PMID:25480348 · one of two readings recorded this
serum TP1NP increase versus control
increases, p = 0.001
In the SrRan + AD3 group, the increase in TP1NP was also statistically significant compared with control (53.3 %, P < 0.001)
PMID:25480348 · one of two readings recorded this
serum TP1NP
TP1NP (ng/nl, mean ± SD) | 0.294 ± 0.06 | 0.304 ± 0.11 | 0.304 ± 0.07 | 0.414 ± 0.10 | 0.304 ± 0.07 | 0.458 ± 0.11
PMID:25480348 · one of two readings recorded this
“up and go” test time, percent reduction
decreases
Thus, to perform the “up and go” test before therapy, patients required on average 15.88 ± 0.95 s compared with 13.48 ± 0.82 s after 6 months of therapy, a 14.26 % reduction
PMID:25480348 · one of two readings recorded this
“up and go” test time
“Up and go” test (s, mean ± SD) | 15.26 ± 3.14 | 15.06 ± 3.06 | 15.74 ± 3.45 | 15.69 ± 3.41 | 15.88 ± 3.80 | 13.48 ± 3.28
PMID:25480348 · one of two readings recorded this
cartilage volume loss, femur (MRI)
p = 0.809
Femur | -7.70 ± 2.66 | -6.98 ± 4.26 | -7.28 ± 2.91 | 0.809*
PMID:25888851 · one of two readings recorded this
cartilage volume loss, femur (MRI)
p = 0.02
Femur | -6.39 ± 3.36 | -5.26 ± 2.92 | 0.020 | -6.16 ± 2.97 | -8.57 ± 2.32 | 0.028
PMID:25888851 · one of two readings recorded this
cartilage volume loss, femur (MRI)
p = 0.171
Femur | -6.15 ± 3.29 | -7.28 ± 2.91 | 0.171
PMID:25888851 · one of two readings recorded this
cartilage volume loss, global knee (MRI)
p = 0.351
Global knee | -7.66 ± 2.10 | -6.67 ± 2.56 | -8.02 ± 3.28 | 0.351*
PMID:25888851 · one of two readings recorded this
cartilage volume loss, global knee (MRI)
p = 0.227
Global knee | -6.75 ± 2.81 | -6.50 ± 2.71 | 0.227 | -6.89 ± 3.70 | -9.33 ± 2.19 | 0.066
PMID:25888851 · one of two readings recorded this
cartilage volume loss, global knee (MRI)
p = 0.034
Global knee | -6.70 ± 2.78 | -8.02 ± 3.28 | 0.034
PMID:25888851 · one of two readings recorded this
cartilage volume loss, global plateau (MRI)
decreases, p = 0.017
Ext+ BML+ patients in the SrRan 1 g/day group demonstrated a significant reduction in cartilage volume loss in the global plateau (P = 0.017) and in the SrRan 2 g/day group in the medial plateau (P = 0.046), compared with placebo
PMID:25888851 · one of two readings recorded this
cartilage volume loss, lateral plateau
decreases, p = 0.019
the Ext+ patients demonstrated that both SrRan 1 g/day and 2 g/day significantly reduced the cartilage volume loss in the lateral plateau (-7.29% ± 3.86, P = 0.019 and -6.46% ± 3.93, P = 0.014, respectively) compared to placebo (-10.90% ± 5.08)
PMID:25888851 · one of two readings recorded this
cartilage volume loss, lateral plateau
decreases, p = 0.014
the Ext+ patients demonstrated that both SrRan 1 g/day and 2 g/day significantly reduced the cartilage volume loss in the lateral plateau (-7.29% ± 3.86, P = 0.019 and -6.46% ± 3.93, P = 0.014, respectively) compared to placebo (-10.90% ± 5.08)
PMID:25888851 · one of two readings recorded this
cartilage volume loss, lateral plateau
increases, p = 0.011
Data further showed that the Ext+ patients also had more cartilage volume loss in the lateral plateau than the Ext- patients (-10.90% ± 5.08 versus -8.57% ± 4.95, P = 0.011)
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial compartment (MRI), multivariate adjusted
p = 0.12
In multivariate analysis adjusted as described above, a numerical trend (P = 0.12) toward more cartilage volume loss in the medial compartment in Ext+ patients was found with statistical significance at the medial femur (P = 0.053)
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial compartment (MRI)
p = 0.119
Medial compartment | -10.29 ± 3.68 | -9.14 ± 3.27 | -10.40 ± 4.23 | 0.119*
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial compartment (MRI)
p = 0.09
Medial compartment | -7.08 ± 4.33 | -9.57 ± 5.29 | 0.090 | -9.69 ± 5.50 | -11.22 ± 1.90 | 0.103
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial compartment (MRI)
p = 0.0005
Medial compartment | -7.60 ± 4.63 | -10.40 ± 4.23 | 0.0005
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial femur (MRI), multivariate adjusted
p = 0.053
In multivariate analysis adjusted as described above, a numerical trend (P = 0.12) toward more cartilage volume loss in the medial compartment in Ext+ patients was found with statistical significance at the medial femur (P = 0.053)
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial femur (MRI)
p = 0.29
Medial femur | -11.17 ± 4.25 | -10.72 ± 5.36 | -10.89 ± 3.19 | 0.290*
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial femur (MRI)
p = 0.055
Medial femur | -7.54 ± 4.90 | -9.26 ± 4.03 | 0.055 | -10.72 ± 4.08 | -11.08 ± 1.86 | 0.339
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial femur (MRI)
p = 0.0002
Medial femur | -7.90 ± 4.76 | -10.89 ± 3.19 | 0.0002
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial plateau (MRI)
p = 0.048
Medial plateau | -8.13 ± 5.98 | -4.90 ± 5.19 | -9.07 ± 8.74 | 0.048* | 0.708** | 0.081**
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial plateau (MRI)
p = 0.708
Medial plateau | -8.13 ± 5.98 | -4.90 ± 5.19 | -9.07 ± 8.74 | 0.048* | 0.708** | 0.081**
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial plateau (MRI)
decreases, p = 0.046
Ext+ BML+ patients in the SrRan 1 g/day group demonstrated a significant reduction in cartilage volume loss in the global plateau (P = 0.017) and in the SrRan 2 g/day group in the medial plateau (P = 0.046), compared with placebo
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial plateau (MRI)
p = 0.081
Medial plateau | -8.13 ± 5.98 | -4.90 ± 5.19 | -9.07 ± 8.74 | 0.048* | 0.708** | 0.081**
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial plateau (MRI)
p = 0.185
Medial plateau | -5.79 ± 5.68 | -10.46 ± 11.70 | 0.185 | -7.04 ± 10.97 | -11.45 ± 4.47 | 0.155
PMID:25888851 · one of two readings recorded this
cartilage volume loss, medial plateau (MRI)
p = 0.012
Medial plateau | -6.77 ± 7.52 | -9.07 ± 8.74 | 0.012
PMID:25888851 · one of two readings recorded this
cartilage volume loss per additional co-localized factor, femur (MRI)
p = 0.239
Femur | -0.53 | 0.239
PMID:25888851 · one of two readings recorded this
cartilage volume loss per additional co-localized factor, global knee (MRI)
p = 0.033
Global knee | -0.86 | 0.033
PMID:25888851 · one of two readings recorded this
cartilage volume loss per additional co-localized factor, medial compartment (MRI)
p = 0.0005
Medial compartment | -2.22 | 0.0005
PMID:25888851 · one of two readings recorded this
cartilage volume loss per additional co-localized factor, medial femur (MRI)
p = 0.002
Medial femur | -1.95 | 0.002
PMID:25888851 · one of two readings recorded this
cartilage volume loss per additional co-localized factor, medial plateau (MRI)
p = 0.006
Medial plateau | -2.93 | 0.006
PMID:25888851 · one of two readings recorded this
cartilage volume loss per additional co-localized factor, plateau (MRI)
p = 0.007
Plateau | -1.97 | 0.007
PMID:25888851 · one of two readings recorded this
cartilage volume loss, plateau (MRI), multivariate adjusted
decreases, p = 0.014
SrRan at 2 g/day demonstrated a significant reduction in cartilage volume loss in the global plateau in both univariate (P = 0.007, Table 6) and multivariate analyses (P = 0.014, data not shown)
PMID:25888851 · one of two readings recorded this
cartilage volume loss, plateau (MRI)
p = 0.003
Plateau | -7.61 ± 3.79 | -5.74 ± 3.54 | -10.01 ± 5.79 | 0.003* | 0.070** | 0.007**
PMID:25888851 · one of two readings recorded this
cartilage volume loss, plateau (MRI)
p = 0.07
Plateau | -7.61 ± 3.79 | -5.74 ± 3.54 | -10.01 ± 5.79 | 0.003* | 0.070** | 0.007**
PMID:25888851 · one of two readings recorded this
cartilage volume loss, plateau (MRI)
p = 0.007
Plateau | -7.61 ± 3.79 | -5.74 ± 3.54 | -10.01 ± 5.79 | 0.003* | 0.070** | 0.007**
PMID:25888851 · one of two readings recorded this
cartilage volume loss, plateau (MRI)
p = 0.162
Plateau | -7.38 ± 4.15 | -9.40 ± 7.49 | 0.162 | -8.67 ± 7.12 | -11.57 ± 3.37 | 0.093
PMID:25888851 · one of two readings recorded this
cartilage volume loss, plateau (MRI)
p = 0.005
Plateau | -7.80 ± 5.05 | -10.01 ± 5.79 | 0.005
PMID:25888851 · one of two readings recorded this
joint space width loss, multivariate adjusted
p = 0.021
This result was further confirmed in multivariate regression (P = 0.021)
PMID:25888851 · one of two readings recorded this
joint space width loss per additional co-localized factor
p = 0.0001
% | -11.58 | <0.0001
PMID:25888851 · one of two readings recorded this
Sources cited
4 papers
- Subject
- strontium(2+)
- Findings
- 6
- Papers
- 4
Efficacy and safety of strontium ranelate in the treatment of knee osteoarthritis: results of a double-blind, randomised placebo-controlled trial.record2013PMID:231172451 finding
Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis.record2012PMID:221245752 findings
Vertebral anti-fracture efficacy of strontium ranelate according to pre-treatment bone turnover.record2010PMID:194369411 finding
Strontium ranelate for preventing and treating postmenopausal osteoporosis.record2006PMID:170542532 findings