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Trial · NCT00869206

Outcomes12

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercentage of Participants With at Least One Skeletal-related Event (SRE) Within 2 Years After Randomization2 yearsAll patients that were eligible and completed treatment were analyzed.percentage of participantsNUMBER
SECONDARYAverage Pain Intensity Score as Assessed by the Brief Pain Inventory (BPI) Questionnairefrom baseline up to 2 years1766 patients completed treatment and were analyzed.score on a scaleMEAN
SECONDARYAverage ECOG Performance Statusfrom baseline up to 2 years1766 patients completed treatment and were analyzed.score on a scaleMEAN
SECONDARYIncidence of Osteonecrosis of the Jawfrom baseline up to 2 years1766 patients completed treatment and were analyzed.percentage of participantsNUMBER
SECONDARYIncidence of Renal Dysfunctionfrom baseline up to 2 years1689 patients completed treatment and were analyzed.percentage of participantsNUMBER
SECONDARYSkeletal Morbidity Ratefrom baseline up to 2 years1766 patients were treated and analyzed.SRE's per yearMEAN
SECONDARYBone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Breast Cancer)from baseline up to 2 years266 breast cancer patients who were treated and included in this portion of the substudy.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Breast Cancerfrom baseline up to 24 months820 patients completed treatment and were analyzed.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Prostate Cancerfrom baseline up to 24 months660 patients completed treatment and were analyzed.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Patients Having at Least One SRE Within 24 Months After Randomization for the Subgroups of Patients With Multiple Myelomafrom baseline up to 24 months265 patient completed treatment and were analyzed.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYBone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Prostate Cancer)from baseline up to 24 months207 prostate cancer patients who were treated and included in this portion of the substudy.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYBone Turnover Assessed by Serum C-telopeptide (CTX) Levels (Multiple Myeloma)from baseline up to 24 months74 multiple myeloma patients were treated and included in this portion of the substudy.ParticipantsCOUNT_OF_PARTICIPANTS

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.

For software

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GET https://conductscience.org/api/trials/v1/NCT00869206/outcomes