Plain-English translation of NCT02418442 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This study is building a comprehensive database of children with rheumatic diseases like juvenile arthritis and lupus. Researchers will collect information about the treatments these children receive and how safe and effective those treatments are over time. By gathering information from many children across multiple medical centers, researchers hope to answer important questions about which medications work best and which ones might cause problems.
Most existing studies of individual medications are too small to spot rare but serious side effects, don't track children long enough to find delayed problems, and can't fairly compare treated children to untreated ones. This registry aims to solve those problems by following many children over years to get a clearer, safer picture of how rheumatic disease treatments actually work in real life.
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You would join a long-term registry where your medical information—including details about your diagnosis, treatments, and how you're doing—gets recorded by your rheumatology care team. You and your family may be contacted periodically to provide updates or answer questions about your health and medications. There is no specific medication or procedure you'll be asked to take or do as part of this study; it's about sharing information that's already part of your regular medical care to help researchers learn from many children's experiences over time.
AI-generated summary from trial data · Aug 29, 2026 · Not medical advice
United States