ID

4709

Beskrivning

Nyckelord

  1. 2011-11-11 2011-11-11 -
  2. 2014-03-21 2014-03-21 - Martin Dugas
Uppladdad den

21 mars 2014

DOI

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Licens

Creative Commons BY-NC 3.0 Legacy

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Eligibility Criteria NCT00035451 AF

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion criteria
Beskrivning

Inclusion criteria

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

History of atrial fibrillation

Datatyp

boolean

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

Cardioversion

Datatyp

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
Beskrivning

Anticoagulation

Datatyp

boolean

Alias
UMLS CUI-1
C0449867
Exclusion criteria
Beskrivning

Exclusion criteria

Previously unsuccessful electrical cardioversions
Beskrivning

Previous cardioversions

Datatyp

boolean

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

Antiarrhythmic drugs

Datatyp

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
Beskrivning

Qualifying arrhythmia

Datatyp

boolean

Alias
UMLS CUI-1
C0003811

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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