Stress Urinary Incontinence for Female Patients (CGM MUIT-2301)

Recruiting N/A Interventional Study
Stress Urinary Incontinence (SUI)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
19 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
96 (estimated)
Sponsor
Ceragem Clinical Inc. · Industry
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About This Trial

This study is a multicenter, prospective, randomized, double-blind, sham-controlled clinical trial conducted in female patients with stress urinary incontinence.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with urine leakage of ≥1 g on the standardized pad test Exclusion Criteria: * Patients with mixed urinary incontinence with predominant urgency urinary incontinence * Patients with stress urinary incontinence * Patients with overflow urinary incontinence
Contacts

Myeongbae Shin, Researcher

82-10-4373-2808

mbshin94@ceragem.com

CONTACT