Possibia

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