Mesh Reinforcement During Temporary Stoma Closure After Sphincter-Saving Rectal Cancer Surgery (NCT02576184) | Clinical Trial Compass
CompletedNot Applicable
Mesh Reinforcement During Temporary Stoma Closure After Sphincter-Saving Rectal Cancer Surgery
France381 participantsStarted 2015-12
Plain-language summary
This study aim to assess long-term results of an incisional hernia-prophylactic mesh placement during stoma reversal after total mesorectal excision (TME) for rectal cancer
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age \> 18
* Operated on for diverting ileostoma closure after sphincter saving rectal cancer surgery, irrespective of the time delay between ileostoma closure and rectal cancer surgery
* Signed consent
* Affiliation to the French social security system
Exclusion Criteria:
* Emergency surgery
* History of laparotomy before ileostoma closure.
* Surgery associated to the ileostoma closure, excluding appendectomy or liver biopsy
* Lactating or pregnant woman
* Allergy to porcine product or collagen-based product. Allergy to polypropylene.
* Participation to another protocol focusing on ileostoma closure