4829175
Last Update Posted: 2025-05-23
Recruiting
Females accepted | 21 Years + |
1000 Estimated Participants | No Expanded Access |
Observational Study | Does not accept healthy volunteers |
Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry
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.
Eligibility
Relevant conditions:
Stress Urinary Incontinence
Pelvic Organ Prolapse
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.
locations
Contact Information
Overall Contact
Christine Romanowski
cromanow@its.jnj.com
908-808-6219
Data sourced from ClinicalTrials.gov