U.S., Feb. 28 -- ClinicalTrials.gov registry received information related to the study (NCT07440927) titled 'Stress Urinary Incontinence for Female Patients (CGM MUIT-2301)' on Feb. 02.
Brief Summary: This study is a multicenter, prospective, randomized, double-blind, sham-controlled clinical trial conducted in female patients with stress urinary incontinence.
Study Start Date: Dec. 13, 2024
Study Type: INTERVENTIONAL
Condition:
Stress Urinary Incontinence (SUI)
Intervention:
DEVICE: 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 ...