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Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

The 50 most recent of 64 record versions are accounted for below. See every version on ClinicalTrials.gov ↗

  1. Re-verified, no change to tracked fieldsv64
  2. Site details revised at 1 of 10 sitesv63
  3. 3 versions Re-verified since Apr 9, 2026, no change to tracked fieldsv60-v62
  4. Primary completion date: Mar 30, 2036 to Mar 31, 2033
    • Study completion date: Aug 30, 2036 to Mar 31, 2038
    • Start date: Apr 13, 2022 to Apr 11, 2022
    v59
  5. Re-verified, no change to tracked fieldsv58
Show 43 earlier versionsHide 43 earlier versions
  1. Study sites: 11 to 10v57
  2. 3 versions Re-verified since Oct 9, 2025, no change to tracked fieldsv54-v56
  3. Site details revised at 1 of 11 sitesv53
  4. 25 versions Re-verified since Jul 18, 2023, no change to tracked fieldsv28-v52
  5. Primary completion date: Aug 29, 2033 to Mar 30, 2036
    • Study completion date: Feb 27, 2034 to Aug 30, 2036
    • Study sites revised (11)
    v27
  6. 11 versions Re-verified since Jul 11, 2022, no change to tracked fieldsv16-v26
  7. Site details revised at 3 of 11 sitesv15
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Ethicon, Inc.
9 trials monitored
See 1 trial at risk
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.
Trial Details
NCT Number NCT04829175
Lead Sponsor Ethicon, Inc.
Conditions
(from sponsor)		 Stress Urinary Incontinence, Pelvic Organ Prolapse
Related terms Pelvic Organ Prolapse, Urinary Incontinence, Stress
Enrollment 1,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov