Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery

NARecruitingINTERVENTIONAL
Enrollment

106

Participants

Timeline

Start Date

May 12, 2025

Primary Completion Date

November 12, 2025

Study Completion Date

November 12, 2025

Conditions
Stress Urinary IncontinenceFemale Urinary IncontinencePelvic Floor Dysfunction
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.

Trial Locations (1)

65090

RECRUITING

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

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Izzet Celegen

OTHER

NCT06924450 - Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery | Biotech Hunter | Biotech Hunter