GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study
NCT: NCT04829058 · RECRUITING
Brief Summary
The objective of this retrospective and prospective, single-arm, observational, multicenter, post-market study is to evaluate outcomes in women who underwent surgery for vaginal or uterine prolapse with a GYNEMESH PS Mesh.
Frequently Asked Questions
What is GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study?
GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study is a clinical trial registered under NCT04829058. Current status: RECRUITING.
What is the status of NCT04829058?
The current status of NCT04829058 (GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study) is: RECRUITING.
When did GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study start?
GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study started on 2021-11-24.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.