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Clinical trialNCT05063331Active, not recruitingInterventional

Patient-Centered Outcomes in the Surgical Treatment of Uterovaginal Prolapse

SponsorUniversity Hospitals Cleveland Medical CenterEnrollment300Uterine Prolapse
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

7 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Mayo Clinic

    Jacksonville, Florida, United States

  • Northwestern Medicine

    Chicago, Illinois, United States

  • Duke University

    Durham, North Carolina, United States

  • Cleveland Clinic

    Cleveland, Ohio, United States

  • Metrohealth Medical Center

    Cleveland, Ohio, United States

  • University Hospitals Cleveland Medical Center

    Cleveland, Ohio, United States

  • University of Pittsburgh, Upmc Magee-Womens Hospital

    Pittsburgh, Pennsylvania, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
15 Dec 2021
Primary completion
31 May 2029
Completion
31 May 2029
Last update posted
15 May 2026
Registered enrollment
300
Registry id
NCT05063331

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.