Mesh-free Suture Urethropexy for Treating Stress Urinary Incontinence, Efficacy and Durability Trial
Recruiting in Palo Alto (17 mi)
GR
Overseen byGhazaleh Rostami Nia, MD
Age: 18+
Sex: Female
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Academic
Waitlist Available
Sponsor: Endeavor Health
No Placebo Group
Trial Summary
What is the purpose of this trial?
In this proposed study, the investigators aim to evaluate a modified suture urethropexy technique for the treatment of female stress urinary incontinence. Participants will be followed with postoperative visits after 2 weeks, 2 months, and 12 months. Pelvic floor ultrasound imaging will be performed before surgery and after 2 months and 12 months, to evaluate urethral mobility.
Research Team
GR
Ghazaleh Rostami Nia, MD
Principal Investigator
Endeavor Health
Eligibility Criteria
Inclusion Criteria
18 years or older with stress dominant urinary incontinence
Stress urinary incontinence confirmed by testing (e.g. urodynamics)
Able to provide informed consent and attend post-operative visits
Treatment Details
Interventions
- Mesh-free Suture Urethropexy (Suture Urethropexy)
Find a Clinic Near You
Research Locations NearbySelect from list below to view details:
NorthShore University HealthSystemSkokie, IL
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Who Is Running the Clinical Trial?
Endeavor Health
Lead Sponsor
Trials
135
Patients Recruited
742,000+
NorthShore University HealthSystem
Lead Sponsor
Trials
134
Patients Recruited
740,000+