ID
20983
Description
RATe Control in Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00313157
Lien
https://clinicaltrials.gov/show/NCT00313157
Mots-clés
Versions (1)
- 02/04/2017 02/04/2017 -
Téléchargé le
2 avril 2017
DOI
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Licence
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
Type de données
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
Type de données
boolean
Alias
- UMLS CUI [1]
- C0010068
- UMLS CUI [2]
- C0018801
Description
systolic blood pressure
Type de données
boolean
Alias
- UMLS CUI [1]
- C0871470
Description
av-conduction disturbance
Type de données
boolean
Alias
- UMLS CUI [1]
- C0004245
Description
hepatic or renal dysfunction
Type de données
boolean
Alias
- UMLS CUI [1]
- C0086565
- UMLS CUI [2]
- C3279454
Description
thyrotoxicosis
Type de données
boolean
Alias
- UMLS CUI [1]
- C0040156
Description
treatment with digitalis
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013216
- UMLS CUI [1,2]
- C0012253
Description
pregnancy or lactation
Type de données
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])