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Trial · NCT00103740

Results by group22

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

OutcomeGroupCategoryValueSpreadUnits
Number of Patients Who Had Therapeutic Response at 6 MonthsZoledronic Acid and Placebo to Risedronate84participants
Number of Patients Who Had Therapeutic Response at 6 MonthsRisedronate and Placebo to Zoledronic Acid67participants
Relative Change in Serum Alkaline Phosphatase in U/L at Day 28Zoledronic Acid and Placebo to Risedronate-49.1Standard Deviation 14.55percent change
Relative Change in Serum Alkaline Phosphatase in U/L at Day 28Risedronate and Placebo to Zoledronic Acid-24.3Standard Deviation 18.19percent change
Relative Change in Serum C-telopeptide (CTx) in ng/mL at Day 10Zoledronic Acid and Placebo to Risedronate-74.2Standard Deviation 123.73percent change
Relative Change in Serum C-telopeptide (CTx) in ng/mL at Day 10Risedronate and Placebo to Zoledronic Acid-40.1Standard Deviation 34.70percent change
Relative Change in Urine α-CTx in ug/mmol at Day 10Zoledronic Acid and Placebo to Risedronate-87.5Standard Deviation 39.33percent change
Relative Change in Urine α-CTx in ug/mmol at Day 10Risedronate and Placebo to Zoledronic Acid-28.7Standard Deviation 68.22percent change
Time to First Therapeutic ResponseZoledronic Acid and Placebo to Risedronate64Inter-Quartile Range 33 to 65days
Time to First Therapeutic ResponseRisedronate and Placebo to Zoledronic Acid91Inter-Quartile Range 64 to 181days
Number of Patients Who Achieved Serum Alkaline Phosphatase Normalization at Day 28Zoledronic Acid and Placebo to Risedronate8participants
Number of Patients Who Achieved Serum Alkaline Phosphatase Normalization at Day 28Risedronate and Placebo to Zoledronic Acid1participants
Change in Pain Severity at Day 182Zoledronic Acid and Placebo to Risedronate-0.5Standard Deviation 1.74units on a scale
Change in Pain Severity at Day 182Risedronate and Placebo to Zoledronic Acid-0.1Standard Deviation 2.02units on a scale
Change in Pain Interference at Day 182Zoledronic Acid and Placebo to Risedronate-0.5Standard Deviation 1.97units on a scale
Change in Pain Interference at Day 182Risedronate and Placebo to Zoledronic Acid0.0Standard Deviation 1.89units on a scale
Number of Participants With a Loss of Therapeutic Response During the Extended Observation PeriodZoledronic Acid and Placebo to Risedronate102218 to NAparticipants
Number of Participants With a Loss of Therapeutic Response During the Extended Observation PeriodRisedronate and Placebo to Zoledronic Acid42344 to 1605participants
Number of Participants With a Partial Disease Relapse During the Extended Observation PeriodZoledronic Acid and Placebo to Risedronate92218 to NAparticipants
Number of Participants With a Partial Disease Relapse During the Extended Observation PeriodRisedronate and Placebo to Zoledronic Acid37373 to 1652participants

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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