drugset / Trial / NCT05169593

Prevention of Postoperative Endoscopic Recurrence With Endoscopy-driven Versus Systematic Biological Therapy

NCT05169593

Phase 4 Recruiting 292 enrolled Universitaire Ziekenhuizen KU Leuven
RandomizedParallel-groupOpen-labelPrevention

Summary

With this prospective, randomized, multicentre, parallel group pragmatic non-inferiority trial, the investigators will evaluate if endoscopy-driven introduction of biological therapy is not leading to more postoperative endoscopic recurrence at week 86 compared to systematic prophylactic biological therapy in patients with CD undergoing an ileocolonic resection with ileocolonic anastomosis. Secondary analyses will include influence on clinical, biological and surgical CD recurrence, serious adverse events, direct costs, work productivity, and quality of life. If the investigators can demonstrate the non-inferiority of an endoscopy-driven approach, this patient-tailored management could be advocated, while a more expensive systematic introduction of biological therapies could be limited. Finally, endoscopic images provided through the SOPRANO CD study, will be used to develop a new scoring system evaluating postoperative endoscopic recurrence.

Timeline

Start
2022-09-08
Primary completion
2027-10
Completion
2030-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject Infliximab Monoclonal antibody 5 mg/kg Intravenous
Subject Infliximab Monoclonal antibody 120 mg Intravenous
Subject Risankizumab Monoclonal antibody 360 mg Subcutaneous
Subject Ustekinumab Monoclonal antibody 90 mg Subcutaneous
Subject Vedolizumab Monoclonal antibody 108 mg Intravenous
Subject Vedolizumab Monoclonal antibody 300 mg Intravenous

Indications