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Terminated No phase listed Observational

Exair® Versus Native Tissue Repair for Prolapse

ClinicalTrials.gov ID: NCT02162628

Public ClinicalTrials.gov record NCT02162628. 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 22, 2026, 12:21 PM EDT

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

Official title

Exair® Prolapse Repair System Versus Native Tissue Repair for Treatment of Pelvic Organ Prolapse, Exair 522 Study

Study identification

NCT ID
NCT02162628
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Coloplast A/S
Industry
Enrollment
79 participants

Conditions and interventions

Interventions

  • Exair Prolapse Repair System Device
  • Total Native Tissue Repair 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
Jul 31, 2014
Primary completion
Nov 30, 2015
Completion
Nov 30, 2015
Last update posted
Dec 13, 2015

2014 – 2015

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Progressive GYN Center Savannah Georgia 31405
Women's Health Advantage Fort Wayne Indiana 46825
Advanced Urogynecology of Michigan Dearborn Michigan 48124
Minnesota Women's Care Maplewood Minnesota 55109
Atlantic Urogynecology Associates Morristown New Jersey 07960
Princeton Urogynecology Princeton New Jersey 08540
Albany Medical Center Albany New York 12208
United Health Services Johnson City New York 13790
Lyndhurst Clinical Research Winston-Salem North Carolina 27103
Novant Health Clinical Research Winston-Salem North Carolina 27103
The Institute for Female Pelvic Medicine and Reconstructive Surgery Allentown Pennsylvania 18103
Vermont Urogynecology Associates, P.C. Williston Vermont 05495
Carillion Clinic OB/GYN Christiansburg Virginia 24073

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02162628, 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 Dec 13, 2015 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02162628 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →