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Primary Prevention of Peristomial Hernias Via Parietal Prostheses — GRECCAR 07  

Parastomal Hernia Clinical Trial

Official title:
Primary Prevention of Peristomial Hernias Via Parietal Prostheses: a Randomized, Multicentric Study

Clinical Trial Summary

The purpose of this study is to compare rates of hernia formation between colostomies created with no hernia preventing mesh versus colostomies created with a particular mesh.

Clinical Trial Description

Previous studies indicate that implanting mesh for peristomal hernia repair may efficiently prevent hernia relapse. However, mesh provides a good infection site, which is not a desirable characteristic for a material adjacent to a colostomy "port". Our goal is to implement a high-quality, randomized trial to demonstrate whether or not systematic mesh implantation upon primary hernia creation is an effective means of avoiding this common and troublesome complication. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01380860
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Completed
Phase N/A
Start date November 2012
Completion date October 20, 2018
View Details
See also
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