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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04829058
Study type Observational
Source Ethicon, Inc.
Contact Christine Romanowski
Phone 908-808-6219
Email cromanow@its.jnj.com
Status Recruiting
Phase
Start date November 24, 2021
Completion date March 31, 2032

See also
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