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NCT04829175

Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry

Recruiting now Last updated 13 April 2026
What this trial tests

trial testing Intervention in Stress Urinary Incontinence in 1,000 participants. Currently enrolling.

Timeline
11 April 2022
Primary endpoint
31 March 2033
31 March 2038

Quick facts

Lead sponsorEthicon, Inc.
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment1,000
Start date11 April 2022
Primary completion31 March 2033
Estimated completion31 March 2038
Sites10 locations across France, Denmark, Italy, Austria, Sweden, Germany, United States

Drugs / interventions tested

Conditions studied

Sponsor

Ethicon, Inc. — full company profile →

Who can join

21 and older, female only, with Stress Urinary Incontinence or Pelvic Organ Prolapse. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this post market, clinical registry is to evaluate the performance of the products of the TVT family of products or vaginal vault or uterine prolapse repair (with laparotomic or laparoscopic approach including robotic assisted) using either Gynemesh PS Mesh or Artisyn Mesh in women undergoing surgery for SUI and POP.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Intervention

Trials testing the same drug.

Other recruiting trials for Stress Urinary Incontinence

Currently open trials in the same condition.

Other Ethicon, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04829175.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing