๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-12

Patient-Centered Outcomes in the Surgical Treatment of Uterovaginal Prolapse (NCT05063331)

Patient-Centered Outcomes of Sacrocolpopexy Versus Uterosacral Ligament Suspension for the Treatment of Uterovaginal Prolapse

๐Ÿ”ต Active, Not Recruiting Observational / Diagnostic ๐Ÿฉบ Clinical Procedure Protocol Sponsor: University Hospitals Cleveland Medical Center

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The purpose of this study is to compare two types of surgery for the treatment of uterovaginal prolapse to determine which surgery works best from a patient's perspective and has the lowest number of short-term and long-term complications.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic โ€” Jacksonville, Florida

Age range: 18 Years to 80 Years

๐Ÿงช Interventions in This Study

  • Minimally invasive supracervical hysterectomy and sacrocolpopexy (MI-SCH+SCP) (PROCEDURE)
  • Vaginal hysterectomy with uterosacral ligament suspension (TVH+USLS) (PROCEDURE)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (7 Sites)

  • Mayo Clinic โ€” Jacksonville, Florida
  • Northwestern Medicine โ€” Chicago, Illinois
  • Duke University โ€” Durham, North Carolina
  • University Hospitals Cleveland Medical Center โ€” Cleveland, Ohio
  • MetroHealth Medical Center โ€” Cleveland, Ohio
  • Cleveland Clinic โ€” Cleveland, Ohio
  • University of Pittsburgh, UPMC Magee-Womens Hospital โ€” Pittsburgh, Pennsylvania

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ 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 ยง 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.

Explore by condition: All Uterine Prolapse clinical trials

๐Ÿ’ก 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.
๐Ÿ›๏ธ View Official NIH Record โ†—