Follow-up study for women who received mesh for prolapse surgery
Part of Women’s health & pregnancy clinical trials.
This study is checking women’s outcomes after a specific prolapse surgery where a mesh material (GYNEMESH PS) was used. If you had this operation and can do follow-up visits, this study may help doctors better understand the mesh’s real-world safety and results.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are female and had laparoscopic or open abdominal sacrocolpopexy for uterine or top-of-vagina prolapse
- Your surgeon used GYNEMESH PS mesh as a “bridging” material during that operation
- You are willing and able to come for follow-up
- You (or your authorized representative) signed the study consent form
- You were at least 21 years old when you signed consent
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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