Trials / Recruiting
RecruitingNCT07276295
Synthetic Versus Autologous Sling For Stress Incontinence
Synthetic Versus Autologous Sling For Stress Incontinence (SASSI): A Randomized Controlled Trial
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 232 (estimated)
- Sponsor
- University of British Columbia · Academic / Other
- Sex
- Female
- Age
- 60 Years
- Healthy volunteers
- Not accepted
Summary
This is a multi-centre randomized controlled trial comparing mid-urethral synthetic mesh sling or tension-free vaginal tape (TVT) and autologous fascia sling (AFS) in elderly patients with stress predominant urinary incontinence. The investigators aim to investigate new onset pelvic pain 6 months post-op and objective urinary incontinence cure rate 5 years post-op. Secondary objectives include investigation of opioid use, mental health, sexual health, and other post-op outcomes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | autologous fascia sling | Participants will receive autologous fascia sling as surgery for stress predominant urinary incontinence. |
| PROCEDURE | tension-free vaginal tape | Participants will receive tension-free vaginal tape as surgery for stress predominant urinary incontinence. |
Timeline
- Start date
- 2026-01-12
- Primary completion
- 2032-06-01
- Completion
- 2032-12-01
- First posted
- 2025-12-11
- Last updated
- 2026-01-16
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT07276295. Inclusion in this directory is not an endorsement.