Plain-English translation of NCT04243525 on ClinicalTrials.gov โ ยท Source last updated ยท Translation generated ยท How we translate trials
This is a research registry โ essentially a secure database โ where patients with inflammatory bowel disease (Crohn's disease or ulcerative colitis) can choose to contribute their medical records. By sharing your information with researchers at the University of Pittsburgh, you'll help scientists learn more about what causes these conditions and how disease patterns differ from person to person. This information may also help researchers identify patients for future studies testing new treatments.
Inflammatory bowel disease affects millions of people, but doctors still don't fully understand what causes it or why it affects different people in different ways. By collecting medical information from many patients in one place, researchers hope to spot patterns that could lead to better, more personalized treatments and eventually ways to prevent the disease.
You likely qualify ifโฆ
You likely don't qualify ifโฆ
Participation is straightforward: you'll sign a consent form giving researchers permission to include your medical records in the registry. After that, your information will be stored securely and used for research studies โ you won't need to visit the clinic more often or undergo any new tests. Researchers may also contact you in the future to see if you're interested in participating in other studies related to inflammatory bowel disease.
AI-generated summary from trial data ยท Jun 2, 2026 ยท Not medical advice
United States