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Peristomal Hernia Rate 5 Years After a Terminal Colostomy With the Parietex ™ TCM Parietal Prosthesis Versus Without Mesh — RESEDAE  

Parastomal Hernia Clinical Trial

Official title:
Peristomal Hernia Rate 5 Years After a Terminal Colostomy With the Parietex ™ TCM Parietal Prosthesis Versus Without Mesh: Material-epidemiology Study

Clinical Trial Summary

This study is a follow-up of the GRECCAR 07 cohort (NCT01380860). Patients will be evaluated 5 years following terminal colostomy to observe patient long-term patient outcomes from colostomy with and without mesh placement.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04282473
Study type Observational
Source Centre Hospitalier Universitaire de Nimes
Contact Michel Prudhomme, MD
Phone 06.43.50.35.22
Email michel.prudhomme@chu-nimes.fr
Status Recruiting
Phase
Start date May 24, 2022
Completion date May 2024
View Details
See also
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