ID
16895
Beschrijving
Triple III Comparison of Leflunomide Alone Versus Two DMARD Combinations in the Treatment of Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00579878
Link
https://clinicaltrials.gov/show/NCT00579878
Trefwoorden
Versies (1)
- 13-08-16 13-08-16 -
Geüploaded op
13 augustus 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00579878
Eligibility Rheumatoid Arthritis NCT00579878
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Leflunomide
Datatype
boolean
Alias
- UMLS CUI [1]
- C0063041
Beschrijving
Methotrexate in combination with study drugs
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0025677
- UMLS CUI [1,2]
- C0304229
Beschrijving
Hypersensitivity: Study Drug
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0304229
Beschrijving
Steroids: Dosage
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0038317
- UMLS CUI [1,2]
- C0178602
Beschrijving
Grade of disease and rheumatoid lung disease
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0441800
- UMLS CUI [1,2]
- C0003873
- UMLS CUI [2]
- C2889132
Beschrijving
Comorbidity
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
Beschrijving
Alcohol consumption
Datatype
boolean
Alias
- UMLS CUI [1]
- C0001948
Beschrijving
Gynaecological status
Datatype
boolean
Alias
- UMLS CUI [1]
- C3831118
- UMLS CUI [2]
- C0700589
Beschrijving
Cognitive Function and Informed Consent
Datatype
boolean
Alias
- UMLS CUI [1]
- C0392335
- UMLS CUI [2]
- C0021430
Similar models
Eligibility Rheumatoid Arthritis NCT00579878
- StudyEvent: Eligibility
C0242801 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0003873 (UMLS CUI [1,2])
C2889132 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
C0021430 (UMLS CUI [2])
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