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Clinical Trial Summary

We will get the impact of duloxetine versus imipramine on therapeutic efficacy in women with SUI.


Clinical Trial Description

Background/Purpose: Pharmacologic treatments for female stress urinary incontinence (SUI) include duloxetine and imipramine. Duloxetine and Imipramine has been reported to have clinical significant therapeutic efficacy on female SUI and overactive bladder syndrome. However, there was no randomized controlled study to compare duloxetine and imipramine for the treatment of female SUI. Patients and Methods: We will perform a prospective randomized controlled study to recruit 90 female SUI patients at the Obstetrics & Gynecology outpatient clinic of Far Eastern Memorial Hospital. All SUI female patients will be asked to complete ICIQ-UI, USS, OABSS, and bladder diary before and after 4 weeks' duloxetine versus imipramine treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05677295
Study type Interventional
Source Far Eastern Memorial Hospital
Contact Sheng-Mou Hsiao, MD
Phone +886289667000
Email smhsiao2@gmail.com
Status Recruiting
Phase Phase 3
Start date April 18, 2023
Completion date December 31, 2024