Role of Mesh in Laparoscopic Sacropexy Surgical Techniques for the Treatment of Female Genital Prolapse

Recruiting now

Conditions studied: Female Genital Prolapse

In brief

This study aims to determine the rate of recurrence of central pelvic organ prolapse in patients who have undergone surgery (sacropexy with and without mesh) for the same pathology.

Key facts

Study ID

NCT06720831

Run by

IRCCS Azienda Ospedaliero-Universitaria di Bologna

People needed

160

Starts

2024-12-01

Expected to finish

2025-03-01

Last updated by the study team

2024-12-06

Who can join

Age: 18 and older, up to 80. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years
• Clinical diagnosis of genital prolapse stage ≥ 2 according to POP-Q classification
• Surgical treatment of laparoscopic sacropexy by mesh (group 1) and without (group 2) in female patients
• Acquisition of informed consent
• At least one follow-up evaluation at 24 months

You may not qualify if…

• Age > 80 years
• Previous genital prolapse surgery

Where it is running

• IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna, Bologna, Italy (enrolling)
• Azienda Ospedaliera Universitaria Integrata di Verona — Verona, Verona, Italy

Full record on ClinicalTrials.gov

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