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
Inclusion Criteria3
- 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 Criteria4
- 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
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Locations(16)
View Full Details on ClinicalTrials.gov
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NCT04282473