About this trial
Prospectively study the correlation between Leucine-rich α2-glycoprotein (LRG) and clinical/endoscopic/histological disease activity in patients with inflammatory bowel disease (IBD) in Europe.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
≥18 years
Patient with confirmed diagnosis of IBD
Patient with planned endoscopy (ileocolonoscopy for Crohn's disease (CD)/ulcerative colitis (UC) or sigmoidoscopy for UC) for the assessment of endoscopic disease activity according to routine practice
willing to provide informed consent
Disqualifiers
Patient with IBD unspecified
Patient with ileo- or colostomy
Patient with total colectomy
Women that are pregnant
Trial population
patients with IBD
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
Leucine-rich α2-glycoprotein
Diagnostic testLeucine-rich α2-glycoprotein measurement
Treatment groups
Trial outcomes
Primary outcomes
Correlation between LRG serum level and endoscopic disease activity in CD and UC
Correlation between LRG serum level and endoscopic disease activity in CD and UC
Sponsors and contacts
Click on the lead sponsor to view all of their trials.