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Trial · NCT00869206

Results by group30

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With at Least One Skeletal-related Event (SRE) Within 2 Years After RandomizationArm I (Zoledronic Acid Every 4 Weeks)67.6percentage of participants
Percentage of Participants With at Least One Skeletal-related Event (SRE) Within 2 Years After RandomizationArm II (Zoledronic Acid Every 12 Weeks)67.9percentage of participants
Average Pain Intensity Score as Assessed by the Brief Pain Inventory (BPI) QuestionnaireArm I (Zoledronic Acid Every 4 Weeks)2.06Standard Error 0.14score on a scale
Average Pain Intensity Score as Assessed by the Brief Pain Inventory (BPI) QuestionnaireArm II (Zoledronic Acid Every 12 Weeks)2.09Standard Error 0.14score on a scale
Average ECOG Performance StatusArm I (Zoledronic Acid Every 4 Weeks)0.82Standard Error 0.042score on a scale
Average ECOG Performance StatusArm II (Zoledronic Acid Every 12 Weeks)0.84Standard Error 0.042score on a scale
Incidence of Osteonecrosis of the JawArm I (Zoledronic Acid Every 4 Weeks)2.0percentage of participants
Incidence of Osteonecrosis of the JawArm II (Zoledronic Acid Every 12 Weeks)1.0percentage of participants
Incidence of Renal DysfunctionArm I (Zoledronic Acid Every 4 Weeks)1.2percentage of participants
Incidence of Renal DysfunctionArm II (Zoledronic Acid Every 12 Weeks).5percentage of participants
Skeletal Morbidity RateArm I (Zoledronic Acid Every 4 Weeks).4Standard Deviation 1.0SRE's per year
Skeletal Morbidity RateArm II (Zoledronic Acid Every 12 Weeks).4Standard Deviation 1.1SRE's per year
Bone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Breast Cancer)Breast Cancer 4 WeeksLow CTX (<0.415ng/ml)83Participants
Bone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Breast Cancer)Breast Cancer 12 WeeksLow CTX (<0.415ng/ml)75Participants
Bone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Breast Cancer)Breast Cancer 4 WeeksHigh CTX (>0.415ng/ml)54Participants
Bone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Breast Cancer)Breast Cancer 12 WeeksHigh CTX (>0.415ng/ml)54Participants
Proportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Breast CancerBreast Cancer 4 Weeks113Participants
Proportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Breast CancerBreast Cancer 12 Weeks119Participants
Proportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Prostate CancerProstate Cancer 4 Weeks107Participants
Proportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Prostate CancerProstate Cancer 12 Weeks101Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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