Clin2
NCT07497321Likely a fitNot yet recruiting

Pelvic mesh implant for prolapse surgery

Pelvic Organ Prolapse (POP)Synthetic MeshLaparoscopic SurgeryGynecologic Laparoscopic SurgerySacrocolpopexyPelvic Floor ProlapsePelvic FloorImplant

Part of Women’s health & pregnancy clinical trials.

This study tests a new pelvic mesh implant for laparoscopic surgery to treat pelvic organ prolapse. It looks at how safe and well the implant works to support organs that have dropped.

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

Phase
N/A
Enrollment
100 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You are a candidate for surgical repair of pelvic organ prolapse using the ProGYNious mesh.
  • You have symptomatic pelvic organ prolapse (POP-Q stage 2 or higher).
  • You are between 18 and 80 years old.
  • You are willing and able to attend follow-up visits as required.
  • You have no previous or current cancer that could affect treatment with the mesh.
  • You have not had prior mesh surgery for prolapse or urinary incontinence.

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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