Plain-English translation of NCT06606756 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a registry study that gathers health information from children and teenagers with inflammatory bowel disease (IBD) at pediatric hospitals across German-speaking countries. Doctors and researchers use this shared data to better understand how the disease progresses, what treatments work best, and how to improve care for young patients. Your medical information helps build a larger picture of IBD in young people.
Inflammatory bowel disease affects many young people, but doctors still have gaps in understanding how it develops and progresses in children and teenagers. By collecting health information from many patients over time, researchers can identify patterns, improve treatment strategies, and help future young patients receive better care.
You likely qualify if…
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You'll share your medical information with the registry at the start of your care and then during follow-up visits at your hospital. Your doctors will enter your health data (like test results, symptoms, and treatments) into a secure online platform in a way that protects your privacy. This happens as part of your regular care — there are no extra visits or procedures needed just for the study.
AI-generated summary from trial data · Jun 2, 2026 · Not medical advice
Germany
Enrollment target
~6,300 participants
Started
September 2004
Primary completion
December 2034
Last updated on clinicaltrials.gov in September 2024.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Jan de Laffolie, MD
University of Giessen
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.