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A Study Evaluating the Clinical Outcome of a Modified d'Hoore Technique for Laparoscopic Ventral Mesh Rectopexy — POP-01  

Rectal Prolapse Clinical Trial

Official title:
A Prospective Study Evaluating the Clinical Outcome of a Modified d'Hoore Technique for Laparoscopic Ventral Mesh Rectopexy

Clinical Trial Summary

The purpose of this observational study is to evaluate the clinical outcome of a modified d'Hoore technique for laparoscopic ventral mesh rectopexy in patients with primary rectal prolapse, rectocele and/or enterocele.The goal of the study will be achieved by reporting the peri- and postoperative complications ((serious) adverse events), recurrences and re-interventions. Pre-operative to postoperative changes in pain, functional outcome and quality of life will be evaluated as well.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04564677
Study type Observational
Source Duomed
Contact Stephanie De Munter, PhD
Phone +32 (0)11 28 69 48
Email stephanie.de.munter@archerresearch.eu
Status Recruiting
Phase
Start date February 8, 2021
Completion date December 31, 2025
View Details
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