A Study to Evaluate Utilizing MRI for Earlier Diagnosis of Rheumatoid Arthritis

Overview

Información sobre este estudio

The primary purpose of this study is to describe the utilization and findings on magnetic resonance imaging (MRI) of the hands and feet in patients with seronegative rheumatoid arthritis (RA) (based on the ACR 1987 or 2010 classification criteria) compared to the findings seen in patients with seropositive disease (RF or ACPA positive).

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Age ≥ 18 years.
  • Undifferentiated inflammatory arthritis suspected to be early rheumatoid arthritis (RA) by the evaluating clinician with clinical synovitis of ≥ 1 joint and ≥ 1 other tender joint but not fulfilling classification criteria.
  • Symptom duration ≤ 2 years.
  • Arthralgias suspected to be early RA by the evaluating clinician without clinical evidence of synovitis.

Exclusion Criteria:

  • Unwillingness or inability to return to Mayo Clinic for research follow-up visits.
  • Current or previous (within the previous 6 months) use ofDMARDs – prednisone (≥ 10 mg/day), methotrexate,hydroxychloroquine, sulfasalazine, leflunomide, adalimumab, certolizumab, etanercept, golimumab, infliximab, abatacept, tocilizumab, sarilumab, tofacitinib, rituximab, or anakinra.
  • Contraindications to contrast-enhanced MRI ( renal insufficiency with estimated GFR ≤ 60 ml/min/1.73 m², extreme claustrophobia, metal implants or devices that contraindicate MRI).
  • Contraindications to contrast-enhanced PCD-CT (eGFR < 30, history of previous contrast allergic reaction, history of premedication prior to iodinated contrast).
  • Personal history of another definite autoimmune or inflammatory rheumatic disease (e.g., rheumatoid arthritis, systemic lupus erythematosus, polymyositis, dermatomyositis, vasculitis, gout, or CPPD) diagnosed by a rheumatologist, excluding secondary Sjogren’s syndrome.
  • Women who are pregnant or nursing.
  • Personal history of psoriasis diagnosed by a primary care physician or dermatologist.
  • Personal history of inflammatory bowel disease diagnosed by a gastroenterologist.
  • Unsuitability to participate in the judgment of a study investigator.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Kerry Wright, M.B.B.S.

Cerrado para la inscripción

Contact information:

Kathleen McCarthy-Fruin M.S.

(507) 284-4797

McCarthy-Fruin.Kathleen@mayo.edu

More information

Publicaciones

Publications are currently not available
.
CLS-20450977

Mayo Clinic Footer