drugset / Trial / NCT01942681
Female Patients With Signs of uRgE and Stress Urinary Incontinence Study of Propiverine Hydrochloride
Completed
62 enrolled
Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan
Shinshu University Hospital · collab
NaSingle-groupOpen-labelTreatment
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.
Timeline
- Start
- 2013-09
- Primary completion
- 2015-06
- Completion
- 2015-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Propiverine | Small molecule | — | — |