Phase
Condition
Idiopathic Inflammatory Myopathies
Rheumatoid Arthritis (Pediatric)
Systemic Lupus Erythematosus
Treatment
N/AClinical Study ID
Ages 2-60 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Rheumatic disease under low immunosuppression (hydroxychloroquine, sulfasalazine ormethotrexate plus prednisone up to 7,5mg/day or leflunomide plus prednisone up to 7,5mg/day),
Resident in high risk área for Yellow Fever
Exclusion
Exclusion Criteria:
Active disease
Primary immunodeficiency
History of anaphylactic response to vaccine components or egg allergy
Living outside the risk area
Do not meet criteria for low immunosuppression
History of previous immunization with the yellow fever vaccine
History of live virus vaccine up to 4 weeks before
Individuals who do not agree to participate in the study and/or whose parents do notagree to participate in the study
Study Design
Connect with a study center
Rheumatology Division of Hospital das Clínicas da Faculdade de Medicina da Universidade de Sao Paulo
São Paulo, Sao Paulo 05403-000
BrazilSite Not Available

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