Multicenter Ventral Mesh Rectopexy Registry Collaborative
Recruiting
Observational Study
Pelvic Organ Prolapse
Rectocele
Enterocele
Rectal Prolapse
Descending Perineum Syndrome
Surgery
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 200 (estimated)
- Sponsor
- University Hospital, Antwerp · Other
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About This Trial
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) ar…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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.
Exclusion Criteria:
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Contacts