ID
20983
Description
RATe Control in Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00313157
Link
https://clinicaltrials.gov/show/NCT00313157
Keywords
Versions (1)
- 4/2/17 4/2/17 -
Uploaded on
April 2, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00313157
Eligibility Atrial Fibrillation NCT00313157
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
hypersensitivity or contraindication to metoprolol, verapamil, diltiazem, carvedilol
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0522473
- UMLS CUI [1,2]
- C0025859
- UMLS CUI [2,1]
- C0522473
- UMLS CUI [2,2]
- C0042523
- UMLS CUI [3,1]
- C0522473
- UMLS CUI [3,2]
- C0012373
- UMLS CUI [4,1]
- C0522473
- UMLS CUI [4,2]
- C0054836
Description
coronary heart disease or heart failure
Data type
boolean
Alias
- UMLS CUI [1]
- C0010068
- UMLS CUI [2]
- C0018801
Description
systolic blood pressure
Data type
boolean
Alias
- UMLS CUI [1]
- C0871470
Description
av-conduction disturbance
Data type
boolean
Alias
- UMLS CUI [1]
- C0004245
Description
hepatic or renal dysfunction
Data type
boolean
Alias
- UMLS CUI [1]
- C0086565
- UMLS CUI [2]
- C3279454
Description
thyrotoxicosis
Data type
boolean
Alias
- UMLS CUI [1]
- C0040156
Description
treatment with digitalis
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0013216
- UMLS CUI [1,2]
- C0012253
Description
pregnancy or lactation
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Similar models
Eligibility Atrial Fibrillation NCT00313157
- StudyEvent: Eligibility
C0741285 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
C0025859 (UMLS CUI [1,2])
C0522473 (UMLS CUI [2,1])
C0042523 (UMLS CUI [2,2])
C0522473 (UMLS CUI [3,1])
C0012373 (UMLS CUI [3,2])
C0522473 (UMLS CUI [4,1])
C0054836 (UMLS CUI [4,2])
C0018801 (UMLS CUI [2])
C3279454 (UMLS CUI [2])
C0012253 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])