🏛️ Verified NIH Record • Updated 2026-03-26
A Study to Assess the Safety and Effectiveness of the UrOActive® Artificial Urinary sPHincter (AUS) (NCT06968741)
Study to Assess the Safety and Effectiveness of the UrOActive® Artificial Urinary sPHincter In the treAtment of Stress Urinary Incontinence in Men
🟢 Recruiting Observational / Diagnostic ⚙️ Medical Device Protocol Sponsor: UroMems SAS
🩺 Plain-English Summary (8th-Grade Level)
Prospective, multicenter, single-arm study
Who can join: Review the eligibility criteria below.
Location: University of California, Los Angeles — Los Angeles, California
Age range: 22 Years
🧪 Interventions in This Study
📋 "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 (21 Sites)
- University of California, Los Angeles — Los Angeles, California
- University of California, San Francisco — San Francisco, California
- Stanford University — Stanford, California
- Minnesota Urology — Bloomington, Minnesota
- Mayo Clinic — Rochester, Minnesota
- Wake Forest University of Health Sciences — Charlotte, North Carolina
- Duke University — Durham, North Carolina
- Cleveland Clinic Foundation — Cleveland, Ohio
- Vanderbilt University Medical Center — Nashville, Tennessee
- Urology Clinics of North Texas — Dallas, Texas
- University of Texas, Southwestern — Dallas, Texas
- University of Texas, MD Anderson — Houston, Texas
- Urology of Virginia — Virginia Beach, Virginia
- Centre Hospitalier Universitaire de Lille — Lille,
- Hospitals Academics De Marseille Conception — Marseille,
- Centre Hospitalier Universitaire de Nantes — Nantes,
- Groupe Hospitalier Pitié-Salpêtrière — Paris,
- Centre Hospitalier Univeritaire de Lyon - Hôpital Lyon Sud — Pierre-Bénite,
- Centre Hospitalier Universitaire de Rennes — Rennes,
- Centre Hospitalier Universitaire de Rouen — Rouen,
- Hopital Foch — Suresnes,
📞 Contact the Study Coordinator
Phone: (469) 766-9888
Email: roshini.jain@uromems.com
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 Stress Urinary Incontinence (SUI)
Explore by condition: All Stress Urinary Incontinence (SUI) 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.