Mesh implant for keyhole surgery to repair pelvic organ prolapse
Part of Women’s health & pregnancy clinical trials.
This study tests a new mesh implant (a small piece of medical fabric) that is placed during keyhole surgery to support the pelvic organs and treat prolapse. The goal is to see if it is safe and works well for patients with this condition.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have pelvic organ prolapse that is causing symptoms (like a bulge or pressure) and is at least stage 2 on the POP-Q scale.
- You are older than 18 and 80 or younger.
- You have not had any previous surgery using mesh for prolapse or urinary incontinence.
- You have no history of cancer that might affect the success of the mesh treatment.
- You are not pregnant or breastfeeding, and you don't have a known allergy to polypropylene (the mesh material).
- You are willing and able to come to follow-up visits after the procedure.
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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