drugset / Trial / NCT00928070

A Study Of Efficacy And Safety Of Fesoterodine In Vulnerable Elderly Subjects With Overactive Bladder

NCT00928070 ↗

Phase 4 Completed 566 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is designed to assess the efficacy and safety of a flexible dose regimen of fesoterodine on urgency urinary incontinence (UUI) episodes in vulnerable elderly subjects with overactive bladder (OAB).

Timeline

Start
2009-09
Primary completion
2011-09
Completion
2011-09

Outcome

Met primary endpoint

paper At week 12 the fesoterodine group had significantly greater improvements in urgency urinary incontinence episodes per 24 hours (-2.84 vs -2.20, p = 0.002) PMID 23973522 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Fesoterodine Other / unclassified 4 mg —
Subject Fesoterodine Other / unclassified 8 mg —

Indications