Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry
NCT: NCT04829175 · RECRUITING
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.
Frequently Asked Questions
What is Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry?
Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry is a clinical trial registered under NCT04829175. Current status: RECRUITING.
What is the status of NCT04829175?
The current status of NCT04829175 (Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry) is: RECRUITING.
When did Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry start?
Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry started on 2022-04-11.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.