Observational Study of Pediatric Rheumatic Diseases: The CARRA Registry
- Study HIC#:2000023073REG
- Last Updated:04/21/2023
Brief Summary:
Continuation of the CARRA Registry as described in the protocol will support data collection on patients with pediatric-onset rheumatic diseases. The CARRA Registry will form the basis for future CARRA studies. In particular, this observational registry will be used to answer pressing questions about therapeutics used to treat pediatric rheumatic diseases, including safety questions.
- Age2 years - 21 years
- GenderBoth
Contact Us
For more information about this study, including how to volunteer, contact:
Catherine Tsao
- Phone Number: 1-203-785-4390
Help Us Discover!
You can help our team find trials you might be eligible for by creating a volunteer profile in MyChart. To get started, create a volunteer profile, or contact helpusdiscover@yale.edu, or call +18779788343 for more information.
Trial Purpose and Description
1. Prospectively collect essential data from children, adolescents and young adults with pediatric onset rheumatic diseases.
2. Evaluate the safety of therapeutic agents in persons with pediatric onset rheumatic diseases.
Eligibility Criteria
Study Population
Children with pediatric rheumatic diseases enrolled from participating CARRA sites.
Criteria
Inclusion Criteria:
1.Onset of rheumatic disease prior to age 16 years for JIA and onset prior to age 19 years for all other rheumatic diseases (see appendix A).
2.Subject (and/or parent/legal guardian when required) is able to provide written informed consent and willing to comply with study procedures.
3.Subject and/or parent/legal guardian can read either English or Spanish.
4.Subject and/or parent/legal guardian is willing to be contacted in the future by study staff.
Exclusion Criteria:
1. Greater than 21 years of age at the time of enrollment.
