The CARRA Registry

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This is an observational registry of children and young adults with pediatric-onset rheumatic conditions such as juvenile idiopathic arthritis (JIA) and Systemic Lupus Erythematosus (SLE) and SLE-like conditions. The registry will be used to answer questions about how safe medications are, how well medications work, and how well patients do over time. Patients who agree to participate will allow their health information to be used for research, complete a brief questionnaire during their clinic visits, and in some cases, be asked to give a sample of blood, urine, cheek swabs, stool, leftover (from clinical procedure) joint fluid, and leftover (from clinical procedure) tissue biopsy.

Who Do I Contact?

If you are interested in participating in the study or want to learn more please contact our study team at rrc [at] chop.edu or 267-426-8726.

Eligibility & Criteria

IRB #:
15-012012
Official Title:
Observational Study of Pediatric Rheumatic Diseases: The CARRA Registry
Study Phase:
Not Applicable
Eligible Age Range:
0 - 18 Years
Gender:
All
Study Categories: