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NCT07530484: SUI-SLING
Sling Insertion Angle and Outcomes in Single-Incision Midurethral Sling Surgery
trial in Stress Urinary Incontinence (SUI) in 184 participants. Completed in 31 October 2019.
31 October 2019
Quick facts
| Lead sponsor | Shin Kong Wu Ho-Su Memorial Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 184 |
| Start date | 1 October 2017 |
| Primary completion | 31 October 2019 |
| Estimated completion | 31 October 2019 |
| Sites | 1 location across Taiwan |
Conditions studied
- Stress Urinary Incontinence (SUI) — all drugs for Stress Urinary Incontinence (SUI) →
- Female Stress Urinary Incontinence — all drugs for Female Stress Urinary Incontinence →
Sponsor
Shin Kong Wu Ho-Su Memorial Hospital
Who can join
18 and older, female only, with Stress Urinary Incontinence (SUI) or Female Stress Urinary Incontinence. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07530484
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Stress Urinary Incontinence (SUI)
Currently open trials in the same condition.
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- NCT07075900 — Dynamic Neuromuscular Stabilization vs Pelvic Floor Muscle Training in Women With Stress Urinary Incontinence · NA · recruiting
- NCT07009249 — Dynamic Neuromuscular Stabilization Exercises in Women With Urinary Incontinence · NA · recruiting
- NCT06623617 — The Impact of Breathing Training on PPSUI: A Randomized Controlled Trial · NA · recruiting
Other Shin Kong Wu Ho-Su Memorial Hospital trials
Trials by the same sponsor.
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- NCT07207356 — Ultrasound Guided Transcutaneous Pulsed Radiofrequency for Cervical Radiculopathy · NA · recruiting
- NCT07032051 — Continuous Passive Motion to Prevent Ankle Contracture and Muscle Atrophy in Ventilated Patients · NA · not yet recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07530484 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Shin Kong Wu Ho-Su Memorial Hospital
- Last refreshed: 15 April 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07530484.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing