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Stress Urinary Incontinence for Female Patients (CGM MUIT-2301)
Sponsor: Ceragem Clinical Inc.
Summary
This study is a multicenter, prospective, randomized, double-blind, sham-controlled clinical trial conducted in female patients with stress urinary incontinence.
Official title: A Multi-center, Prospective, Randomized, Double-blind, Sham Device Controlled Clinical Trial to Compare and Evaluate the Efficacy and Safety of the Use an Investigational Device (Model Name CGM MUIT-2301) and Sham Device (Model Name CGM MUIT-2301C) for Female Patients With Stress Urinary Incontinence
Key Details
Gender
FEMALE
Age Range
19 Years - Any
Study Type
INTERVENTIONAL
Enrollment
96
Start Date
2024-12-13
Completion Date
2026-09-30
Last Updated
2026-02-27
Healthy Volunteers
No
Conditions
Interventions
Ceragem Innerfit medi-tech
Stress Urinary Incontinence Device (Ceragem Innerfit medi-tech) The investigational device and control device were applied at least 5 days per week, twice daily (morning and evening), for 15 minutes per session, over a total period of 12 weeks.
Locations (1)
Samsung Seoul Hospital
Seoul, South Korea