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

Centre Hospitalier Universitaire de Nīmes134 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

134

Conditions

Colostomy Stoma Parastomal Hernia

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * The patient must be affiliated with a health insurance programme * Patient was included in the GRECCAR 07 cohort (PHRC National 2011; N° RCB: 2011-A01572-39 - ClinicalTrials.gov ID: NCT01380860) * Patient received colostomy 5 years ago Exclusion Criteria: * The subject is participating in another category I interventional study, or is in a period of exclusion determined by a previous study * The subject signals opposition to participating in the study * The patient is under safeguard of justice or state guardianship * The patient is pregnant or breastfeeding

Locations (16)

L'Hôpital Jean Minjoz

Besançon, France

RECRUITING

CHU de Bordeaux

Bordeaux, France