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Terminated Phase 4 Interventional

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

ClinicalTrials.gov ID: NCT02123992

Public ClinicalTrials.gov record NCT02123992. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 6:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Safety and Efficacy Cohort Study of Elevate® Apical and Posterior Prolapse Repair System Compared to Native Tissue Repair for Pelvic Organ Prolapse Repair

Study identification

NCT ID
NCT02123992
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
ASTORA Women's Health
Industry
Enrollment
99 participants

Conditions and interventions

Interventions

  • Elevate Apical and Posterior Device
  • Native Tissue Repair for pelvic organ prolapse Procedure

Device · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2014
Primary completion
Mar 31, 2019
Completion
Mar 31, 2019
Last update posted
Sep 6, 2016

2014 – 2019

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
Urological Associates of Southern Arizona Tucson Arizona 85941
The Clark Center for Urogynecology Newport Beach California 92663
Yale School of Medicine New Haven Connecticut 06520
National Center for Advanced Pelvic Surgery Washington D.C. District of Columbia 20010
Women's Health Advantage Fort Wayne Indiana 46825
Metro Urology Woodbury Minnesota 55125
Adult & Pediatric Urology and Urogynecology Omaha Nebraska 68114
Women's Cancer Center of Nevada Las Vegas Nevada 89169
Delaware Valley Urology Mount Laurel New Jersey 08054
Princeton Medical Center Princeton New Jersey 08540
The Center for Specialized Women's Health Whippany New Jersey 07981
North Shore Women's Health Clinic Great Neck New York 11021
Premier Medical Group Poughkeepsie New York 12601
The Institute for Female Pelvic Medicine - St. Luke's Hospital Allentown Pennsylvania 18103
Center for Women's Health of Lansdale Lansdale Pennsylvania 19446
The Female Pelvic Health Center Newtown Pennsylvania 18940
Swan Urogynecology Nashville Tennessee 37203
The Womens Centre Denton Texas 76210
University of Texas at Galveston Galveston Texas 77555
Lone Star Urogynecology and Continence Center Round Rock Texas 78665
Female Pelvic Medicine Institute of Virginia North Chesterfield Virginia 23235
Athena Women's Health Issaquah Washington 98027
University of Washington Pelvic Health Center Seattle Washington 98195

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02123992, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 6, 2016 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02123992 live on ClinicalTrials.gov.

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