ID
31986
Description
A Study to Evaluate the Efficacy of Tacrolimus in Rheumatoid Arthritis Patients Shown Unsuccessful Response to Methotrexate; ODM derived from: https://clinicaltrials.gov/show/NCT01224418
Link
https://clinicaltrials.gov/show/NCT01224418
Keywords
Versions (1)
- 10/10/18 10/10/18 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
October 10, 2018
DOI
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License
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT01224418
Eligibility Rheumatoid Arthritis NCT01224418
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Pregnancy | Breast Feeding | Pregnancy, Planned | Breast Feeding Planned
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
- UMLS CUI [3]
- C0032992
- UMLS CUI [4,1]
- C0006147
- UMLS CUI [4,2]
- C1301732
Description
Tacrolimus | Ointment Excluded
Data type
boolean
Alias
- UMLS CUI [1]
- C0085149
- UMLS CUI [2,1]
- C0028912
- UMLS CUI [2,2]
- C0332196
Description
Renal Insufficiency | Creatinine measurement, serum
Data type
boolean
Alias
- UMLS CUI [1]
- C1565489
- UMLS CUI [2]
- C0201976
Description
Liver Failure | Viral hepatitis | Non-viral hepatitis | Liver Cirrhosis | Aspartate aminotransferase increased | Alanine aminotransferase increased
Data type
boolean
Alias
- UMLS CUI [1]
- C0085605
- UMLS CUI [2]
- C0042721
- UMLS CUI [3]
- C4268643
- UMLS CUI [4]
- C0023890
- UMLS CUI [5]
- C0151904
- UMLS CUI [6]
- C0151905
Description
Pancreatitis | Impaired glucose tolerance | Glucose Complication | Blood glucose measurement ante cibus | Blood glucose measurement Postprandial | Hemoglobin A1c measurement
Data type
boolean
Alias
- UMLS CUI [1]
- C0030305
- UMLS CUI [2]
- C0271650
- UMLS CUI [3,1]
- C0017725
- UMLS CUI [3,2]
- C0009566
- UMLS CUI [4,1]
- C0392201
- UMLS CUI [4,2]
- C1550738
- UMLS CUI [5,1]
- C0392201
- UMLS CUI [5,2]
- C0376674
- UMLS CUI [6]
- C0474680
Description
Heart Disease | Myocardial Ischemia | Cardiac Arrhythmia Treatment required for | Heart failure | Cardiac complication
Data type
boolean
Alias
- UMLS CUI [1]
- C0018799
- UMLS CUI [2]
- C0151744
- UMLS CUI [3,1]
- C0003811
- UMLS CUI [3,2]
- C0332121
- UMLS CUI [4]
- C0018801
- UMLS CUI [5]
- C0161816
Description
Investigational New Drugs
Data type
boolean
Alias
- UMLS CUI [1]
- C0013230
Description
infliximab | adalimumab | leflunomide
Data type
boolean
Alias
- UMLS CUI [1]
- C0666743
- UMLS CUI [2]
- C1122087
- UMLS CUI [3]
- C0063041
Similar models
Eligibility Rheumatoid Arthritis NCT01224418
- StudyEvent: Eligibility
C0872146 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
C0438286 (UMLS CUI [1,3])
C0025677 (UMLS CUI [2,1])
C0438286 (UMLS CUI [2,2])
C0201657 (UMLS CUI [2])
C0332287 (UMLS CUI [1,2])
C1306345 (UMLS CUI [1,3])
C0750480 (UMLS CUI [1,4])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [4,1])
C1301732 (UMLS CUI [4,2])
C0028912 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0201976 (UMLS CUI [2])
C0042721 (UMLS CUI [2])
C4268643 (UMLS CUI [3])
C0023890 (UMLS CUI [4])
C0151904 (UMLS CUI [5])
C0151905 (UMLS CUI [6])
C0271650 (UMLS CUI [2])
C0017725 (UMLS CUI [3,1])
C0009566 (UMLS CUI [3,2])
C0392201 (UMLS CUI [4,1])
C1550738 (UMLS CUI [4,2])
C0392201 (UMLS CUI [5,1])
C0376674 (UMLS CUI [5,2])
C0474680 (UMLS CUI [6])
C0151744 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C0332121 (UMLS CUI [3,2])
C0018801 (UMLS CUI [4])
C0161816 (UMLS CUI [5])
C1122087 (UMLS CUI [2])
C0063041 (UMLS CUI [3])