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Sponsored by: |
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
Information provided by: | National Institutes of Health Clinical Center (CC) |
ClinicalTrials.gov Identifier: | NCT00006333 |
The purpose of this study is to learn more about the causes of rheumatoid arthritis, juvenile rheumatoid arthritis and related conditions and the course of these diseases. Patients in this study will not receive treatment, but may be offered participation in a treatment protocol if an appropriate study is available.
Children and adults of all ages with known or suspected arthritis are eligible for this study. Participants will undergo the following tests and procedures:
Condition |
Arthritis Synovitis |
MedlinePlus related topics: | Juvenile Rheumatoid Arthritis Rheumatoid Arthritis |
Study Type: | Observational |
Official Title: | Studies of the Pathogenesis and Natural History of Arthritis and Related Conditions |
Study Start Date: | September 2000 |
This research protocol will recruit patients with arthritis and related conditions for the purpose of screening patients for treatment protocols, and evaluating the natural history of arthritis and related conditions. Patients will be evaluated clinically, radiographically and serologically, and standardized data will be uniformly collected on all patients. Additional imaging using sensitive MRI methods will be obtained in some patients. The collected blood and tissue will be utilized for laboratory studies to continue research on the pathogenic mechanisms of rheumatoid arthritis and related autoimmune joint diseases. Data from the history and physical examination as well as several disability questionnaires in the adult and pediatric population will be used to phenotypically characterize these patients and assess outcome and functional status. Any medical care recommended or provided to the patients will be consistent with routine standards of practice and provided in consultation with the patient's referring physician.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
No age limits.
History of inflammatory synovitis of at least one or more swollen joints.
Patient's ability and willingness to give informed consent or in the pediatric patients, the parent's willingness to give informed consent and the patient's willingness to assent to the protocol whenever possible.
EXCLUSION CRITERIA:
None if patients fulfill inclusion criteria.
Contact: Patient Recruitment and Public Liaison Office | (800) 411-1222 | prpl@mail.cc.nih.gov |
Contact: TTY | 1-866-411-1010 |
United States, Maryland | |||||
National Institutes of Health Clinical Center, 9000 Rockville Pike | Recruiting | ||||
Bethesda, Maryland, United States, 20892 |
NIH Clinical Center Detailed Web Page 
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Study ID Numbers: | 000222, 00-AR-0222 |
First Received: | October 4, 2000 |
Last Updated: | July 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00006333 |
Health Authority: | United States: Federal Government |
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