ConductScience.org, home

Trial · NCT03492281

Results by group60

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline (CFB) at Week 12 in the Average Number of Micturitions Per 24 Hours in All Overactive Bladder (OAB) ParticipantsPlacebo-1.3Standard Error 0.14micturitions per 24 hours
Change From Baseline (CFB) at Week 12 in the Average Number of Micturitions Per 24 Hours in All Overactive Bladder (OAB) ParticipantsVibegron 75 mg-1.8Standard Error 0.14micturitions per 24 hours
Change From Baseline (CFB) at Week 12 in the Average Number of Micturitions Per 24 Hours in All Overactive Bladder (OAB) ParticipantsTolterodine ER 4 mg-1.6Standard Error 0.15micturitions per 24 hours
CFB at Week 12 in the Average Number of Urge Urinary Incontinence (UUI) Episodes Per 24 Hours in OAB Wet ParticipantsPlacebo: OAB Wet-1.4Standard Error 0.13UUI episodes per 24 hours
CFB at Week 12 in the Average Number of Urge Urinary Incontinence (UUI) Episodes Per 24 Hours in OAB Wet ParticipantsVibegron 75 mg: OAB Wet-2.0Standard Error 0.13UUI episodes per 24 hours
CFB at Week 12 in the Average Number of Urge Urinary Incontinence (UUI) Episodes Per 24 Hours in OAB Wet ParticipantsTolterodine ER 4 mg: OAB Wet-1.8Standard Error 0.14UUI episodes per 24 hours
CFB at Week 12 in the Average Number of Urgency Episodes Over 24 Hours in All OAB ParticipantsPlacebo-2.0Standard Error 0.19urgency episodes over 24 hours
CFB at Week 12 in the Average Number of Urgency Episodes Over 24 Hours in All OAB ParticipantsVibegron 75 mg-2.7Standard Error 0.19urgency episodes over 24 hours
CFB at Week 12 in the Average Number of Urgency Episodes Over 24 Hours in All OAB ParticipantsTolterodine ER 4 mg-2.5Standard Error 0.21urgency episodes over 24 hours
Percentage of OAB Wet Participants With at Least a 75% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Placebo: OAB WetUnadjusted36.8percentage of participants
Percentage of OAB Wet Participants With at Least a 75% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Vibegron 75 mg: OAB WetUnadjusted52.4percentage of participants
Percentage of OAB Wet Participants With at Least a 75% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Tolterodine ER 4 mg: OAB WetUnadjusted47.6percentage of participants
Percentage of OAB Wet Participants With at Least a 75% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Placebo: OAB WetAdjusted for sex32.8percentage of participants
Percentage of OAB Wet Participants With at Least a 75% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Vibegron 75 mg: OAB WetAdjusted for sex49.3percentage of participants
Percentage of OAB Wet Participants With at Least a 75% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Tolterodine ER 4 mg: OAB WetAdjusted for sex42.2percentage of participants
Percentage of OAB Wet Participants With a 100% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Placebo: OAB WetUnadjusted22.5percentage of participants
Percentage of OAB Wet Participants With a 100% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Vibegron 75 mg: OAB WetUnadjusted28.8percentage of participants
Percentage of OAB Wet Participants With a 100% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Tolterodine ER 4 mg: OAB WetUnadjusted26.6percentage of participants
Percentage of OAB Wet Participants With a 100% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Placebo: OAB WetAdjusted for sex19.0percentage of participants
Percentage of OAB Wet Participants With a 100% Reduction From Baseline in UUI Episodes Per 24 Hours at Week 12Vibegron 75 mg: OAB WetAdjusted for sex25.3percentage 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

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03492281/results