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Clinical Trial

GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study

NCT: NCT04829058 · TERMINATED

NCT IDNCT04829058
StatusTERMINATED
Start Date2021-11-24
Completion2026-06-24
SponsorEthicon, Inc. (INDUSTRY)
First posted
Last updated

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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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