Exair® Versus Native Tissue Repair for Prolapse
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.
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
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to compare safety and effectiveness of the Exair Prolapse Repair System for treatment of pelvic organ prolapse to traditional native tissue repair through 36 months of follow-up.
Study identification
- NCT ID
- NCT02162628
- Recruitment status
- Terminated
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 79 participants
Conditions and interventions
Conditions
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
- Aug 2014 (Type not available)
- Primary completion
- Dec 2015 (Actual)
- Completion
- Dec 2015 (Actual)
- Last update posted
- Dec 14, 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 14, 2015 · Synced Oct 21, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT02162628 live on ClinicalTrials.gov.