drugset / Trial / NCT00269724

A Study to Evaluate the Safety and Efficacy of OROS® Oxybutynin Chloride for the Treatment of Urge Urinary Incontinence

NCT00269724

Phase 3 Completed 250 enrolled Alza Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to is to evaluate the safety and efficacy of OROS® oxybutynin chloride in patients being treated for urge urinary incontinence. Oxybutynin is an antispasmodic, anticholinergic medication for the treatment of the symptoms of overactive bladder.

Timeline

Start
1997-03
Primary completion
Completion
1997-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxybutynin Small molecule 5 mg Oral
Subject Oxybutynin Small molecule 10 mg Oral
Subject Oxybutynin Small molecule 15 mg Oral
Subject Oxybutynin Small molecule 20 mg Oral
Subject Oxybutynin Small molecule 25 mg Oral
Subject Oxybutynin Small molecule 30 mg Oral

Indications