Overview

Efficacy and Safety of OROS Oybutynin and TTS Oxybutynin in Middle-Aged and Elderly Women With Urinary Incontinence

Status:
Completed
Trial end date:
1996-12-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to compare the side-effect profile and efficacy of sustained release, OROSĀ® and TTS, dosage forms of oxybutynin with immediate release (IR) oral oxybutynin and with placebo.
Phase:
Phase 3
Details
Lead Sponsor:
Alza Corporation, DE, USA
Treatments:
Mandelic Acids
Oxybutynin