RecruitingNCT04282473

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

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


Sponsor

Centre Hospitalier Universitaire de Nīmes

Enrollment

134 participants

Start Date

May 24, 2022

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with colostomy stoma and parastomal hernia. The study is currently recruiting participants at 16 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(16)

L'Hôpital Jean Minjoz

Besançon, France

CHU de Bordeaux

Bordeaux, France

CHRU Clermont- Ferrand Hôtel -Dieu

Clermont-Ferrand, France

Hôpital Beaujon (AP-HP)

Clichy, France

Hôpital Albert Michallon

Grenoble, France

Centre Oscar Lambret

Lille, France

Centre Hospitalier Lyon-Sud

Lyon, France

Centre Régional de Lutte contre le Cancer Institut Paoli-Calmettes

Marseille, France

Hôpital La Timone, AP-HM

Marseille, France

CRLC Val d'Aurelle - Paul Lamarque

Montpellier, France

Centre Hospitalier Universitaire Hôtel-Dieu - CHU de Nantes

Nantes, France

CHU de Nimes

Nîmes, France

Hôpital Saint Antoine (AP-HP)

Paris, France

Hôpital Pontchaillou

Rennes, France

Hôpital Charles-Nicolle

Rouen, France

Hôpital Purpan - CHU de Toulouse

Toulouse, France

View Full Details on ClinicalTrials.gov

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NCT04282473


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