ID

4709

Descripción

Palabras clave

Versiones (2)
  1. 11/11/11 11/11/11 -
  2. 21/3/14 21/3/14 - Martin Dugas
Subido en

21 de marzo de 2014

DOI

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Licencia

Creative Commons BY-NC 3.0 Legacy
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Eligibility Criteria NCT00035451 AF

Inglés

Eligibility

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion criteria
Descripción

Inclusion criteria

Documented (12-lead ECG) history of symptomatic atrial fibrillation occurring between 48 hours and 6 months before screening
Descripción

History of atrial fibrillation

Tipo de datos

boolean

Alias
UMLS CUI-1
C0004238
UMLS CUI-2
C1623258
procedure of cardioversion (electric shock to correct abnormal rhythm)
Descripción

Cardioversion

Tipo de datos

boolean

Alias
UMLS CUI-1
C0013778
Patient anticoagulated according to the recommendations of the Study Group on Atrial Fibrillation of the European Society of Cardiology guidelines
Descripción

Anticoagulation

Tipo de datos

boolean

Alias
UMLS CUI-1
C0449867
Exclusion criteria
Descripción

Exclusion criteria

Previously unsuccessful electrical cardioversions
Descripción

Previous cardioversions

Tipo de datos

boolean

Alias
UMLS CUI-1
C0013778
Failed to respond to any Class III antiarrhythmic drugs
Descripción

Antiarrhythmic drugs

Tipo de datos

boolean

Alias
UMLS CUI-1
C0003195
Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
Descripción

Qualifying arrhythmia

Tipo de datos

boolean

Alias
UMLS CUI-1
C0003811
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Similar models

Eligibility

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion criteria
History of atrial fibrillation
Item
Documented (12-lead ECG) history of symptomatic atrial fibrillation occurring between 48 hours and 6 months before screening
boolean
C0004238 (UMLS CUI-1)
C1623258 (UMLS CUI-2)
Cardioversion
Item
procedure of cardioversion (electric shock to correct abnormal rhythm)
boolean
C0013778 (UMLS CUI-1)
Anticoagulation
Item
Patient anticoagulated according to the recommendations of the Study Group on Atrial Fibrillation of the European Society of Cardiology guidelines
boolean
C0449867 (UMLS CUI-1)
Item Group
Exclusion criteria
Previous cardioversions
Item
Previously unsuccessful electrical cardioversions
boolean
C0013778 (UMLS CUI-1)
Antiarrhythmic drugs
Item
Failed to respond to any Class III antiarrhythmic drugs
boolean
C0003195 (UMLS CUI-1)
Qualifying arrhythmia
Item
Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
boolean
C0003811 (UMLS CUI-1)
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