Plain-English translation of NCT04191395 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a registry study — a long-term database — designed to collect medical information from people with chronic inflammatory diseases like inflammatory bowel disease, rheumatoid arthritis, spondyloarthritis, psoriasis, and other similar conditions. Researchers want to understand how these diseases evolve, how they're treated, and whether people with one inflammatory condition are at higher risk of developing another. By gathering detailed information from up to 3,000 patients treated at a major hospital in France, this study aims to create the first comprehensive database of its kind to help improve care for these conditions.
Currently, there is no single database in France that tracks patients across these different chronic inflammatory diseases, even though they share common characteristics and patients often have multiple conditions at the same time. This study exists to fill that gap and help doctors understand patterns in how these diseases develop and which treatments work best.
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As a participant, you would allow researchers to access and review your medical records from your ongoing care at the hospital — including information about your diagnosis, treatments, test results, and how your condition has progressed over time. You would not need to take any new medication or undergo special procedures; instead, the study simply documents your existing care. Your participation is ongoing, meaning your medical information would continue to be tracked as part of this long-term registry.
AI-generated summary from trial data · Jun 2, 2026 · Not medical advice
France