🏛️ 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 Checklist

Full 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.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗