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Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery
Sponsor: Izzet Celegen
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
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.
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)