RecruitingNCT05918367

Multicenter Ventral Mesh Rectopexy Registry Collaborative


Sponsor

University Hospital, Antwerp

Enrollment

200 participants

Start Date

Sep 25, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this multicenter observational study is to collect data prospectively of patients with pelvic organ prolapse undergoing ventral mesh rectopexy (as well as rectoceles, entero-/sigmoidoceles/ intussusception/ rectal prolapse or combined) by laparoscopy or robotic surgery and to evaluate the longterm functional outcomes. Secondly complications (mesh erosions, recurrence, reoperations) are evaluated. Following main questions will be analysed - other can follow in consultation with the collaborative 1. Is VMR the technique of choice for treatment of rectoceles? Functional results - recurrence - mesh related complications 2. Has a perineal descent an impact on the functional outcome of ventral mesh rectopexy perfored for external rectal prolaps, internal rectal prolaps, rectocele, enterocele, sigmoidcele or combined pelvic organ prolapse?


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with descending perineum syndrome, enterocele, and other related conditions. The study is currently recruiting participants at 5 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(5)

UZ Brussel

Brussels, Belgium

University Hospital Antwerp

Edegem, Belgium

AZ Jan Palfijn

Ghent, Belgium

Jessa ziekenhuis

Hasselt, Belgium

AZ Delta Roeselare

Roeselare, Belgium

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NCT05918367


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