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Study identifier: NCT06924450 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery

Condition: Stress Urinary Incontinence · Female Urinary Incontinence · Pelvic Floor Dysfunction  ·  Sponsor: Izzet Celegen

PhaseNA
Planned participants106
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Yusuf Başkıran, Doctor  ·  +905419523468  ·  yusuf.baskiran@istinye.edu.tr

Always discuss trial participation with your own doctor first.

Locations (1)

Van Regional Training and Research Hospital, Department of Obstetrics and GynecologyVan, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT06924450