Able to read Informed Consent | Comprehension Informed Consent | Informed Consent
Item
able to read, understand, and sign the informed consent form
boolean
C0586740 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3])
Able to read English Language | Able to write English Language | Able to speak English Language
Item
able to read, write, and speak english
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0564215 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Age
Item
≥18 years of age
boolean
C0001779 (UMLS CUI [1])
Rheumatoid Arthritis
Item
diagnosed with ra within past 24 months (waiver)
boolean
C0003873 (UMLS CUI [1])
Methotrexate Oral
Item
taking oral methotrexate therapy for a minimum of 3 months
boolean
C3216566 (UMLS CUI [1])
Methotrexate | Response Insufficient | Therapy change Anticipated | Change Methotrexate Dosage | Change Drug Administration Route | DMARDs | Biologic DMARDs
Item
considered to have an insufficient response to methotrexate and therefore a candidate for change to therapy, including changing mtx dose or changing route of delivery, or adding or switching dmards (including but not limited to biologic dmards)
boolean
C0025677 (UMLS CUI [1])
C1704632 (UMLS CUI [2,1])
C0231180 (UMLS CUI [2,2])
C3665894 (UMLS CUI [3,1])
C3840775 (UMLS CUI [3,2])
C0392747 (UMLS CUI [4,1])
C0025677 (UMLS CUI [4,2])
C0178602 (UMLS CUI [4,3])
C0392747 (UMLS CUI [5,1])
C0013153 (UMLS CUI [5,2])
C0242708 (UMLS CUI [6])
C4055380 (UMLS CUI [7])
Study Subject Participation Status | Laboratory Procedures
Item
prior exposure of the study center, study physician or study patient to the avise pg laboratory test
boolean
C2348568 (UMLS CUI [1])
C0022885 (UMLS CUI [2])
Parameters Hepatic Abnormal | Parameters Hematologic Abnormal
Item
patients with known abnormal hepatic and or hematological parameters
boolean
C0449381 (UMLS CUI [1,1])
C0205054 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0449381 (UMLS CUI [2,1])
C0205488 (UMLS CUI [2,2])
C0205161 (UMLS CUI [2,3])
Prednisone U/day | Prednisone Equivalent
Item
use of prednisone >10mg/day (or its equivalent)
boolean
C0032952 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
C0032952 (UMLS CUI [2,1])
C0205163 (UMLS CUI [2,2])
Rheumatic disease | Exception Rheumatoid Arthritis Primary
Item
rheumatologic diagnosis other than primary ra
boolean
C0035435 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0003873 (UMLS CUI [2,2])
C0205225 (UMLS CUI [2,3])