ID

20983

Description

RATe Control in Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00313157

Lien

https://clinicaltrials.gov/show/NCT00313157

Mots-clés

  1. 02/04/2017 02/04/2017 -
Téléchargé le

2 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT00313157

Eligibility Atrial Fibrillation NCT00313157

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
persistent or permanent atrial fibrillation with ventricular rate > 80/min at rest and/or > 100/min average at daytime.
Description

atrial fibrillation, ventricular rate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0741285
male or female, age > 18.
Description

gender, age

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
hypersensitivity or contraindication to metoprolol, verapamil, diltiazem or carvedilol.
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
coronary heart disease or heart failure
Description

coronary heart disease or heart failure

Type de données

boolean

Alias
UMLS CUI [1]
C0010068
UMLS CUI [2]
C0018801
systolic blood pressure < 100 mmhg
Description

systolic blood pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0871470
av-conduction disturbance
Description

av-conduction disturbance

Type de données

boolean

Alias
UMLS CUI [1]
C0004245
severe hepatic or renal dysfunction
Description

hepatic or renal dysfunction

Type de données

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C3279454
thyrotoxicosis
Description

thyrotoxicosis

Type de données

boolean

Alias
UMLS CUI [1]
C0040156
ongoing treatment with digitalis
Description

treatment with digitalis

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0012253
pregnancy or lactation
Description

pregnancy or lactation

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Similar models

Eligibility Atrial Fibrillation NCT00313157

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
atrial fibrillation, ventricular rate
Item
persistent or permanent atrial fibrillation with ventricular rate > 80/min at rest and/or > 100/min average at daytime.
boolean
C0004238 (UMLS CUI [1,1])
C0741285 (UMLS CUI [1,2])
gender, age
Item
male or female, age > 18.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
hypersensitivity or contraindication to metoprolol, verapamil, diltiazem, carvedilol
Item
hypersensitivity or contraindication to metoprolol, verapamil, diltiazem or carvedilol.
boolean
C0522473 (UMLS CUI [1,1])
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])
coronary heart disease or heart failure
Item
coronary heart disease or heart failure
boolean
C0010068 (UMLS CUI [1])
C0018801 (UMLS CUI [2])
systolic blood pressure
Item
systolic blood pressure < 100 mmhg
boolean
C0871470 (UMLS CUI [1])
av-conduction disturbance
Item
av-conduction disturbance
boolean
C0004245 (UMLS CUI [1])
hepatic or renal dysfunction
Item
severe hepatic or renal dysfunction
boolean
C0086565 (UMLS CUI [1])
C3279454 (UMLS CUI [2])
thyrotoxicosis
Item
thyrotoxicosis
boolean
C0040156 (UMLS CUI [1])
treatment with digitalis
Item
ongoing treatment with digitalis
boolean
C0013216 (UMLS CUI [1,1])
C0012253 (UMLS CUI [1,2])
pregnancy or lactation
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

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