Clin2
NCT06430931Possibly a fitRecruiting

OviTex vs synthetic graft in robotic prolapse surgery

Colorectal DisordersProlapseProlapse RectalProlapse GenitalProlapse PelvicRectoceleProlapse UterusCystocele

Part of Digestive system, Kidney & urinary, Women’s health & pregnancy clinical trials.

This trial compares a biological mesh made from sheep tissue (OviTex) with a standard synthetic mesh for repairing pelvic organ prolapse during robotic surgery. It aims to see which one works better and has fewer side effects.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
184 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have pelvic organ prolapse and your doctor recommends surgery (VMR or SCR).
  • You are willing to be randomly assigned to receive either the OviTex or synthetic mesh.
  • You can give written permission to use your medical data for the study.
  • You do not have a history of pelvic radiation, previous pelvic mesh implants, or allergies to sheep products.
  • You are not scheduled for a repeat prolapse surgery (redo-rectopexy).

View the official record on ClinicalTrials.gov

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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