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Female Patients With Signs of uRgE and Stress Urinary Incontinence Study of Propiverine Hydrochloride — FRESH  

Urinary Incontinence Clinical Trial

Official title:
Multi-institution Study on Efficacy and Safety of Propiverine Hydrochloride for Female Patients With Urge and Stress Urinary Incontinence

Clinical Trial Summary

This study is to evaluate the efficacy and safety that the occurrence of incontinence is significantly decrease using the propiverine hydrochloride for 200 female patients with mixed (stress and urge) urinary incontinence in one week during a twelve-week treatment period.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01942681
Study type Interventional
Source Translational Research Informatics Center, Kobe, Hyogo, Japan
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date June 2015
View Details
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