Synthetic Versus Autologous Sling For Stress Incontinence (NCT07276295)
Synthetic Versus Autologous Sling For Stress Incontinence (SASSI): A Randomized Controlled Trial
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: St. Paul's Hospital — Vancouver, British Columbia
Age range: 60 Years
🧪 Interventions in This Study
- autologous fascia sling (PROCEDURE)
- tension-free vaginal tape (PROCEDURE)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- St. Paul's Hospital — Vancouver, British Columbia
📞 Contact the Study Coordinator
Phone: (604) 806-9829
Email: judy.fan@phc.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Urinary Incontinence
- Improving Primary Care Access to Urinary Incontinence Treatment for Women Veterans — Birmingham, Alabama
- Group Versus Individual Physiotherapy for Urinary Incontinence in Aging Women — Montreal, Quebec
- A Practice-Based Intervention To Improve Care for a Diverse Population Of Women With Urinary Incontinence — La Jolla, California
- Clinical Study of External Electrical Stimulation for Male Incontinence — Monroe, Connecticut
- Use of Sildenafil for Treatment of Urinary Incontinence — Galveston, Texas
- WI-INTUIT: Bridging Community Based Continence Promotion and Primary Care — San Diego, California
Explore by condition: All Urinary Incontinence clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.