Multicenter Ventral Mesh Rectopexy Registry Collaborative

Status: Recruiting
Location: See all (5) locations...
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of posterior pelvic organ prolaps planned for laparoscopie or robotic ventral mesh rectopexy with or without concomittant surgery.

• All patients 18 years or older and are able to complete a written informed conscent are eligble for inclusion.

Locations
Other Locations
Belgium
UZ Brussel
RECRUITING
Brussels
University Hospital Antwerp
RECRUITING
Edegem
AZ Jan Palfijn
NOT_YET_RECRUITING
Ghent
Jessa ziekenhuis
RECRUITING
Hasselt
AZ Delta Roeselare
RECRUITING
Roeselare
Contact Information
Primary
Sylvie Van den Broeck
sylvie.vandenbroeck@uza.be
003238215744
Backup
Niels Komen
niels.komen@uza.be
00328215007
Time Frame
Start Date: 2023-09-25
Estimated Completion Date: 2032-09-30
Participants
Target number of participants: 200
Sponsors
Leads: University Hospital, Antwerp

This content was sourced from clinicaltrials.gov