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Clinical Trial

Ethicon Pelvic Mesh Post Market Clinical Follow-up Registry

NCT: NCT04829175 · RECRUITING

NCT IDNCT04829175
StatusRECRUITING
Start Date2022-04-11
Completion2038-03-31
SponsorEthicon, Inc. (INDUSTRY)
First posted
Last updated

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.

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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