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A Study of Oxybutynin for the Treatment of Urge Urinary Incontinence — FP1097-002  

Urinary Incontinence, Urge Clinical Trial

Official title:
An Open-Label, Dose Escalating Study to Evaluate the Safety of Intravaginal Oxybutynin in Subjects With Urge Urinary Incontinence

Clinical Trial Summary

The purpose of this study is to determine the safety of three doses of oxybutynin for the treatment of urge urinary incontinence.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00749632
Study type Interventional
Source FemmePharma Global Healthcare, Inc.
Contact
Status Completed
Phase Phase 2
Start date July 2007
Completion date October 2008
View Details
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