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ID

4709

Descrição

Palavras-chave

  1. 11/11/2011 11/11/2011 -
  2. 21/03/2014 21/03/2014 - Martin Dugas
Transferido a

21 de março de 2014

DOI

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Licença

Creative Commons BY-NC 3.0 Legacy

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    Eligibility Criteria NCT00035451 AF

    1. StudyEvent: Eligibility
      1. Eligibility
    Inclusion criteria
    Descrição

    Inclusion criteria

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

    History of atrial fibrillation

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0004238 (Atrial Fibrillation)
    SNOMED
    49436004
    UMLS CUI-2
    C1623258 (Electrocardiography)
    SNOMED
    29303009
    LOINC
    LP6244-0
    procedure of cardioversion (electric shock to correct abnormal rhythm)
    Descrição

    Cardioversion

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0013778 (Electric Countershock)
    SNOMED
    250980009
    LOINC
    LP97905-1
    Patient anticoagulated according to the recommendations of the Study Group on Atrial Fibrillation of the European Society of Cardiology guidelines
    Descrição

    Anticoagulation

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0449867 (Use of anticoagulation)
    SNOMED
    260678004
    Exclusion criteria
    Descrição

    Exclusion criteria

    Previously unsuccessful electrical cardioversions
    Descrição

    Previous cardioversions

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0013778 (Electric Countershock)
    SNOMED
    250980009
    LOINC
    LP97905-1
    Failed to respond to any Class III antiarrhythmic drugs
    Descrição

    Antiarrhythmic drugs

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0003195 (Anti-Arrhythmia Agents)
    SNOMED
    67507000
    Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
    Descrição

    Qualifying arrhythmia

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0003811 (Cardiac Arrhythmia)
    SNOMED
    698247007
    LOINC
    LA7414-1

    Similar models

    Eligibility

    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    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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