RecruitingNot ApplicableNCT07762300

Hybrid Transobturator Tape Versus Conventional Synthetic Tape for Stress Urinary Incontinence

Hybrid Transobturator Tape Versus Conventional Synthetic Tape: A Randomized Controlled Trial Assessing Safety, Efficacy, and Female Sexual Function

Sponsor

Benha University

Enrollment

90 participants

Start Date

Jul 1, 2026

Study Type

INTERVENTIONAL

Conditions

Female Sexual Function Stress Urinary Incontinence (SUI)Transobturator Tape Hybrid Sling

Summary

This randomized controlled trial compares the safety, efficacy, and impact on female sexual function of a novel hybrid transobturator tape (combining an autologous rectus fascia strip with a polypropylene mesh) versus standard synthetic transobturator tape in women undergoing surgery for stress urinary incontinence.

Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Hybrid Transobturator Tape Sling and a procedure called Standard Synthetic Transobturator Tape (TOT) for people with female sexual function, hybrid sling, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREStandard Synthetic Transobturator Tape (TOT)

Outside-in transobturator tape procedure utilizing a full synthetic polypropylene tape positioned tension-free under the mid-urethra.

PROCEDUREHybrid Transobturator Tape Sling

Insertion of a composite graft (autologous rectus fascia strip harvested via a Pfannenstiel incision and sutured between polypropylene tape arms) positioned via the obturator foramen route with the biological tissue directly under the mid-urethra.