Female Patients With Signs of uRgE and Stress Urinary Incontinence Study of Propiverine Hydrochloride
Status:
Completed
Trial end date:
2015-06-01
Target enrollment:
Participant gender:
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.
Phase:
N/A
Details
Lead Sponsor:
Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan Translational Research Informatics Center, Kobe, Hyogo, Japan