Informatie:
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ID
21746
Beschrijving
A Multiple Dose Study to Evaluate Subcutaneous AMG 108 in Subjects With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00293826
Link
https://clinicaltrials.gov/show/NCT00293826
Trefwoorden
Versies (1)
- 27-04-17 27-04-17 -
Geüploaded op
27 april 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00293826
Eligibility Rheumatoid Arthritis NCT00293826
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00293826
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Criteria for Rheumatoid Arthritis
Item
subjects with active rheumatoid arthritis as diagnosed by meeting acr classification criteria for at least 6 months.
boolean
C3273740 (UMLS CUI [1])
MTX Dosage
Item
must be taking mtx consecutively for >/= 12 weeks and at a stable dose of methotrexate at 15-25 mg weekly for at least 4 weeks prior to screening
boolean
C0025677 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
Pharmacotherapy for inflammatory diseases
Item
receipt of commercial or experimental biologic therapies for the treatment of inflammatory disease
boolean
C0013216 (UMLS CUI [1,1])
C1290884 (UMLS CUI [1,2])
C1290884 (UMLS CUI [1,2])
Infection
Item
presence of serious infection
boolean
C0009450 (UMLS CUI [1])
Rheumatoid Arthritis Classification
Item
class iv rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1,1])
C0008902 (UMLS CUI [1,2])
C0008902 (UMLS CUI [1,2])
Tuberculosis
Item
prior or current history of tuberculosis infection or exposure
boolean
C0041296 (UMLS CUI [1])
DMARD
Item
any other dmards other than methotrexate within 6 weeks of screening
boolean
C0242708 (UMLS CUI [1])
Gynaecological Status
Item
pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Live vaccine
Item
receipt of live vaccines within 3 months
boolean
C0042211 (UMLS CUI [1])
Felty Syndrome
Item
felty's syndrome
boolean
C0015773 (UMLS CUI [1])