The CARRA Registry
NCT01697254 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9587
Last updated 2015-11-17
Summary
This CARRA Registry study will create a foundational database for rheumatic diseases of childhood using a novel informatics infrastructure developed as part of the larger clinical project. The creation of a CARRA-wide informatics infrastructure will enable efficient, observational, disease-related data capture across all CARRA sites for pediatric rheumatic diseases. The CARRA Registry study will demonstrate the feasibility of expanding to more data intensive registries for observational studies, comparative effectiveness research, pharmaceutical clinical trials and translational research.
Conditions
- Juvenile Idiopathic Arthritis
- Systemic Lupus Erythematosus
- Mixed Connective Tissue Disease
- Juvenile Ankylosing Spondylitis
- Juvenile Dermatomyositis
- Localized Scleroderma
- Systemic Sclerosis
- Vasculitis
- Sarcoid
- Fibromyalgia, Primary
- Auto-inflammatory Disease
- Idiopathic Uveitis Idiopathic
Sponsors & Collaborators
-
National Institutes of Health (NIH)
collaborator NIH -
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
collaborator NIH -
Arthritis Foundation
collaborator OTHER -
Lupus Foundation of America
collaborator OTHER -
Cure JM Foundation
collaborator UNKNOWN - lead OTHER
Principal Investigators
-
Laura Schanberg, MD · Duke University
-
Norman T Illowite, MD · Children's Hospital at Montefiore
-
Christy Sandborg, MD · Lucile Salter Packard Children's Hospital/Stanford University School of Medicine
-
Carol Wallace, MD · Seattle Children's Hospital/ University of Washington School of Medicine
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-08-31
- Primary Completion
- 2015-10-31
- Completion
- 2015-10-31
Countries
- United States
Study Locations
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