Clinical Trial

Sling Insertion Angle and Outcomes in Single-Incision Midurethral Sling Surgery

Study acronym: SUI-SLING
Completed
View on ClinicalTrials.gov →
Summary
This study aims to evaluate the effect of sling insertion angle on surgical outcomes and quality of life in women with stress urinary incontinence (SUI) undergoing single-incision midurethral sling surgery. Women diagnosed with urodynamic stress urinary incontinence who underwent surgery using a single-incision sling system were included. Patients were categorized into two groups based on sling insertion angle: an acute-angle group (\<45°, resembling a retropubic trajectory) and a standard-angle group (approximately 45°, toward the obturator foramen). The primary outcome was objective cure at 6 months, defined as a negative cough stress test without the need for additional anti-incontinence treatment. Secondary outcomes included objective cure at 1 and 3 months, postoperative voiding difficulty, persistent SUI symptoms, and quality of life assessed using the Incontinence Quality of Life (I-QOL) questionnaire. This study provides clinical evidence on whether sling insertion angle influences early and mid-term outcomes following single-incision midurethral sling surgery.
Trial Details
NCT Number NCT07530484
Lead Sponsor Shin Kong Wu Ho-Su Memorial Hospital
Conditions Stress Urinary Incontinence (SUI), Female Stress Urinary Incontinence
Enrollment 184 participants
Start Date 2017-10-01
Primary Completion 2019-10-31 (estimated)
Study Completion 2019-10-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-15