Clin2
NCT07066761Possibly a fitRecruiting

Safety of a pelvic floor mesh implant for prolapse

Pelvic Organ Prolapse (POP)Genital ProlapseUterus ProlapseLaparoscopic Surgery

Part of Women’s health & pregnancy clinical trials.

This study tests a new mesh implant to fix pelvic organ prolapse (when organs drop down into the vagina). It looks at how safe and well the implant works in women who need surgery for this condition.

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

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

Who can take part

  • You have a moderate or worse prolapse (stage 2 or higher) in one of the three vaginal areas, whether or not you still have your uterus.
  • Your doctor has said surgery is a treatment option for your prolapse.
  • You are willing and able to come in for follow-up appointments after the surgery.
  • You understand the study and have signed a consent form agreeing to participate.
  • You have not had a previous mesh implant for prolapse (in the front or back vaginal wall).
  • You are not pregnant, do not have active cancer in the vagina, cervix, or rectum, and do not have a known allergy to polypropylene (the mesh material).

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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