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Clinical trialNCT02123992TerminatedPhase 4Interventional

Study of the Elevate Apical and Posterior Prolapse Repair System Compared to Native Tissue Repair for Pelvic Organ Prolapse

SponsorASTORA Women's HealthEnrollment99Pelvic Organ Prolapse
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The aim of this study is to further evaluate the safety and efficacy of the Elevate® Apical and Posterior Prolapse Repair System for repair of apical/posterior pelvic organ prolapse in a controlled, post-market cohort study.

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

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

United States
  • Urological Associates of Southern Arizona

    Tucson, Arizona, United States

  • the Clark Center for Urogynecology

    Newport Beach, California, United States

  • Yale School of Medicine

    New Haven, Connecticut, United States

  • National Center for Advanced Pelvic Surgery

    Washington D.C., District of Columbia, United States

  • Women'S Health Advantage

    Fort Wayne, Indiana, United States

  • Metro Urology

    Woodbury, Minnesota, United States

  • Adult & Pediatric Urology and Urogynecology

    Omaha, Nebraska, United States

  • Women'S Cancer Center of Nevada

    Las Vegas, Nevada, United States

  • Delaware Valley Urology

    Mount Laurel, New Jersey, United States

  • Princeton Medical Center

    Princeton, New Jersey, United States

  • the Center for Specialized Women'S Health

    Whippany, New Jersey, United States

  • North Shore Women'S Health Clinic

    Great Neck, New York, United States

  • Premier Medical Group

    Poughkeepsie, New York, United States

  • the Institute for Female Pelvic Medicine - St. Luke'S Hospital

    Allentown, Pennsylvania, United States

  • Center for Women'S Health of Lansdale

    Lansdale, Pennsylvania, United States

  • the Female Pelvic Health Center

    Newtown, Pennsylvania, United States

  • Swan Urogynecology

    Nashville, Tennessee, United States

  • the Womens Centre

    Denton, Texas, United States

  • University of Texas at Galveston

    Galveston, Texas, United States

  • Lone Star Urogynecology and Continence Center

    Round Rock, Texas, United States

  • Female Pelvic Medicine Institute of Virginia

    North Chesterfield, Virginia, United States

  • Athena Women'S Health

    Issaquah, Washington, United States

  • University of Washington Pelvic Health Center

    Seattle, Washington, 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
30 Apr 2014
Primary completion
30 Apr 2019
Completion
30 Apr 2019
Last update posted
7 Sept 2016
Registered enrollment
99
Registry id
NCT02123992

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.