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RECRUITING

GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study

A Retrospective and Long-Term Prospective Post Market Clinical Follow-up (PMCF) Study of the GYNECARE GYNEMESH® PS Nonabsorbable PROLENE® Soft Mesh

NCT04829058•Ethicon, Inc.

View on ClinicalTrials.gov

AI summary by Clareo Health

Generating AI summary...

Conditions

Pelvic Organ Prolapse

Interventions

Intervention

Locations

3

United States

Locations (3)

Institute for Female Pelvic Medicine

North Wales, Pennsylvania, United States

UMPC

Pittsburgh, Pennsylvania, United States

Universitatsklinikum Tubingen

Tübingen, Germany

Key Dates

Start Date

November 24, 2021

Primary Completion Date

September 30, 2031

Completion Date

March 31, 2032

Last Updated

April 13, 2026

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Contacts

Christine Romanowski

CONTACT

908-808-6219 cromanow@its.jnj.com

Sponsors

Lead Sponsor

Ethicon, Inc.

Full Eligibility Criteria

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 13, 2026Data synced to Clareo: April 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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