drugset / Trial / NCT00224146

Transdermal (TDS) Oxybutynin (Oxytrol(r)) in Overactive Bladder

NCT00224146

Phase 4 Completed 2878 enrolled Watson Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This study evaluates changes in health related quality of life outcomes in patients using Oxytrol(r)

Timeline

Start
2004-05
Primary completion
2005-05
Completion
2005-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxybutynin Small molecule 3.9 mg

Indications