KONO-S Anastomosis Compared to Conventional Ileocolonic Anastomosis to Reduce Recurrence in Crohn's Disease (KOALA)
Crohn Disease
About this trial
This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's disease, Kono-S anastomosis, conventional anastomosis, endoscopic recurrence
Eligibility Criteria
Inclusion Criteria: Adult patient ≥ 18 years and ≤75 years With Crohn's disease. Requiring a first ileocolonic resection: fistulizing, abscessed, or stenosing disease or disease refractory to medical treatment. Affiliated to the French social security system. Exclusion Criteria: Previous ileocolonic resection Contraindication to postoperative endoscopy. Anastomosis with a planned defunctioning protective stoma. Emergency surgery (peritonitis). Lack of consent to the study. Pregnant patients. Refusal to participate or inability to provide informed consent. Patient under legal protection (individuals under guardianship by court order)
Sites / Locations
- CHu de Besançon
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Kono-S group
Control group
Kono-S group, in which ileocolonic anastomosis will be performed following the technique described by Kono et al.
Conventional side-to-side ileocolonic anastomosis