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Study identifier: NCT05918367 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Multicenter Ventral Mesh Rectopexy Registry Collaborative

Condition: Pelvic Organ Prolapse · Rectocele · Enterocele  ·  Sponsor: University Hospital, Antwerp

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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?

This description comes directly from the study's public registry record.

Talk to the study team

Sylvie Van den Broeck  ·  003238215744  ·  sylvie.vandenbroeck@uza.be

Niels Komen  ·  00328215007  ·  niels.komen@uza.be

Always discuss trial participation with your own doctor first.

Locations (5)

UZ BrusselBrussels, BelgiumRecruiting
University Hospital AntwerpEdegem, BelgiumRecruiting
AZ Jan PalfijnGhent, BelgiumNot Yet Recruiting
Jessa ziekenhuisHasselt, BelgiumRecruiting
AZ Delta RoeselareRoeselare, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT05918367