Prognostic Indicators and Determinants of the 2-5 Year Outcome in a Cohort of Early Synovitis Patients

Launched by NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES (NIAMS) · Dec 9, 2002

Keywords

ClinConnect Summary

This study will evaluate the 2-5 year outcome of a cohort of 250 patients with early synovitis, who were recruited into protocol 94-AR-0194 (The Pathogenesis of Inflammatory Synovitis: A Study of Early Arthritis). Clinical, radiographic, and functional outcome parameters, particularly those relating to articular damage and functional loss, will be evaluated and related back to clinical, serologic, immunogenetic, and pathologic variables identified at the onset of the arthropathy. A model will be generated which incorporates and weighs the variables in order to determine diagnostic and progn...

Gender

ALL

Eligibility criteria

• • All patients who have been recruited into, and completed, the 1 year follow up of protocol 94-AR-0194.
• FOR ENTRY ONTO 98-AR-0150 JOINT MRI:
• • Patients currently being evaluated at the NIH through Protocol 94-AR-0194 or 98-AR-1050.
• • Must have at least one clinically active arthritic joint that is under consideration for percutaneous needle synovial biopsy.
• • No patients who have any of the following: cardiac pacemakers, auto defribrillators, neural stimulators, aneurysm clips, metallic prostheses, cochlear (ear) implants, any implanted devices (pumps, infusion devices, etc.), metal fragments in the eye, or shrapnel injuries.
• • No patients who exceed the size limitations of the MRI scanner.
• • No patients who suffer from claustrophobia.
• • No patients who have had a previous anaphylactoid reaction to gadolinium-based contrast material.
• • No patients who are currently pregnant.