ID
31974
Description
Study to Characterize Demographics, Compliance, Tolerability and Safety in Patients With Rheumatoid Arthritis, Psoriatic Arthritis and Ankylosing Spondylitis Prescribed Adalimumab (Humira®) as Part of Routine Clinical Care; ODM derived from: https://clinicaltrials.gov/show/NCT01163916
Lien
https://clinicaltrials.gov/show/NCT01163916
Mots-clés
Versions (1)
- 09/10/2018 09/10/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
9 octobre 2018
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT01163916
Eligibility Rheumatoid Arthritis NCT01163916
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Patients Excluded
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0030705
- UMLS CUI [1,2]
- C0332196
Description
Pharmaceutical Preparations At risk Interactions Adalimumab
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1444641
- UMLS CUI [1,3]
- C0687133
- UMLS CUI [1,4]
- C1122087
Description
Hypersensitivity Adalimumab
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C1122087
Description
Pregnancy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032961
Description
Breast Feeding
Type de données
boolean
Alias
- UMLS CUI [1]
- C0006147
Description
Age
Type de données
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
Communicable Diseases | Tuberculosis
Type de données
boolean
Alias
- UMLS CUI [1]
- C0009450
- UMLS CUI [2]
- C0041296
Description
Study Subject Participation Status
Type de données
boolean
Alias
- UMLS CUI [1]
- C2348568
Similar models
Eligibility Rheumatoid Arthritis NCT01163916
- StudyEvent: Eligibility
C1122087 (UMLS CUI [1,2])
C0278329 (UMLS CUI [1,2])
C0750546 (UMLS CUI [1,3])
C0666743 (UMLS CUI [2])
C0205369 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C1122087 (UMLS CUI [2])
C0332196 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,2])
C0687133 (UMLS CUI [1,3])
C1122087 (UMLS CUI [1,4])
C1122087 (UMLS CUI [1,2])
C0041296 (UMLS CUI [2])