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RECRUITING
NCT06924450
NA

Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery

Sponsor: Izzet Celegen

View on ClinicalTrials.gov

Summary

This study is a single-blind, randomized controlled trial evaluating whether changing the width of the surgical tape (mesh) used in transobturator tape (TOT) surgery improves treatment results in women with stress urinary incontinence (SUI). Two mesh widths are being compared: a 1.2 cm mesh (new method) and a 1.0 cm mesh (standard method). The main goal is to find out if the wider mesh leads to better urinary control and fewer complications. Participants will be followed for one year to measure cure rates, symptom improvement, and satisfaction.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

106

Start Date

2025-05-12

Completion Date

2025-11-12

Last Updated

2025-07-11

Healthy Volunteers

No

Interventions

DEVICE

1.2 cm Mesh TOT

Patients in this group will undergo transobturator tape (TOT) surgery using a 1.2 cm monofilament polypropylene mesh. The modified mesh width is being evaluated for its effect on surgical success, symptom improvement, and postoperative complications.

DEVICE

1.0 cm Mesh TOT

Patients in this group will undergo transobturator tape (TOT) surgery using a 1.0 cm monofilament polypropylene mesh, which is the standard procedure. This group serves as a comparator to assess the impact of the modified mesh width.

Locations (1)

Van Regional Training and Research Hospital, Department of Obstetrics and Gynecology

Van, Turkey (Türkiye)