clinical trial · NCT04829175
Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry
Ethicon, Inc.·—·recruiting·n = 1,000
Stress Urinary IncontinencePelvic Organ ProlapseIntervention
brief 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.
started
Apr 11, 2022
primary completion
Mar 31, 2033
completion
Mar 31, 2038
last updated
May 8, 2026
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
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol