Crohn'
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 16 years or older at the time of informed consent Performance Status (ECOG) of 0-2 Patients diagnosed with Croh's disease who are scheduled to undergo intestinal resection and anastomosis, regardless of the number of prior surgeries, surgical approach (open/laparoscopic), or disease phenotype (stricturing/penetrating) Patients not scheduled for proximal stoma construction at the anastomotic site Patients who have provided written informed consent to participate in this study
Exclusion criteria
Exclusion criteria: Malignant disease Patients in whom a discrepancy of more than twofold in bowel lumen diameter Patients in whom intraoperative findings indicated that bowel anastomosis was inappropriate or a proximal stoma was deemed necessary Emergency surgery for bleeding, perforation, or other acute conditions Malnutrition due to prolonged fasting Pregnant or lactating women, or women who are pregnant or intend to become pregnant Patients judged by the principal or sub-investigator to be inappropriate for inclusion in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of anastomotic leakage (all grades according to the Clavien-Dindo classification) | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of perioperative complications (all grades according to the Clavien-Dindo classification), Anastomosis time, Intraoperative blood loss, Operative time, Postoperative length of hospital stay, Endoscopic recurrence rate at 1 year postoperatively, Clinical recurrence rate at 1 and 5 years postoperatively, Reoperation rate at 5 years postoperatively | — |
Countries
Japan
Contacts
Nagoya University Graduate School of Medicine Department of Gastroenterological Surgery