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Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry

Pelvic Organ Prolapse Clinical Trial

Official title:
A Long Term Prospective Observational Post Market Clinical Follow-Up (PMCF) Registry of Ethicon Gynecare Pelvic Mesh Products for The Treatment of Stress Urinary Incontinence and Pelvic Organ Prolapse

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04829175
Study type Observational
Source Ethicon, Inc.
Contact Christine Romanowski
Phone 908-808-6219
Email cromanow@its.jnj.com
Status Recruiting
Phase
Start date April 13, 2022
Completion date August 30, 2036
View Details
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