drugset / Trial / NCT00911937

A Trial To Evaluate The Efficacy And Safety Of Fesoterodine In Patients With Symptoms Of Overactive Bladder Including Nocturnal Urinary Urgency

NCT00911937 ↗

Phase 4 Completed 963 enrolled Pfizer
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is designed to assess the efficacy of a flexible dose regimen of fesoterodine on micturition related nocturnal urgency episodes.

Timeline

Start
2009-08
Primary completion
2011-09
Completion
2011-09

Outcome

Met primary endpoint

registry Placebo vs Fesoterodine; p = 0.0030; Least squares mean difference -0.22 (95% CI -0.37 to -0.08) NCT00911937 ↗

Drugs

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

Indications