0 Evaluaciones

ID

22531

Descripción

ODM derived from http://clinicaltrials.gov/show/NCT00255281

Link

http://clinicaltrials.gov/show/NCT00255281

Palabras clave

  1. 24/02/12 24/02/12 -
  2. 06/06/17 06/06/17 - Martin Dugas
Subido en

6 giugno 2017

DOI

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Licencia

Creative Commons BY 4.0

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    Efficacy and Safety of AZD7009 in the Treatment of Atrial Fibrillation

    Eligibility

    1. StudyEvent: Eligibility
      1. Eligibility
    Einschlusskriterien
    Descripción

    Einschlusskriterien

    Alias
    UMLS CUI-1
    C1512693
    Alter 18 Jahre bis 80 Jahre
    Descripción

    Age

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    Clinical indication for cardioversion of Atrial Fibrillation. Effective oral anticoagulation according to local routines or a TEE without any finding of intracardial thrombus or signs of thrombogenecity
    Descripción

    Atrial Fibrillation Cardioversion

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0741278
    Clinical indication for cardioversion of Atrial Fibrillation. Effective oral anticoagulation according to local routines or a TEE without any finding of intracardial thrombus or signs of thrombogenecity
    Descripción

    anticoagulation

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0449867
    Clinical indication for cardioversion of Atrial Fibrillation. Effective oral anticoagulation according to local routines or a TEE without any finding of intracardial thrombus or signs of thrombogenecity
    Descripción

    TEE

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0206054
    Ausschlusskriterien
    Descripción

    Ausschlusskriterien

    Alias
    UMLS CUI-1
    C0680251
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    Descripción

    Sinus Node Dysfunction

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0428908
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    Descripción

    Atrioventricular nodal disease

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1841659
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    Descripción

    potassium abnormal

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0549635
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    Descripción

    QTc

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0860814
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    Descripción

    QRS

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1880451

    Similar models

    Eligibility

    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Einschlusskriterien
    C1512693 (UMLS CUI-1)
    Age
    Item
    Alter 18 Jahre bis 80 Jahre
    boolean
    C0001779 (UMLS CUI [1])
    Atrial Fibrillation Cardioversion
    Item
    Clinical indication for cardioversion of Atrial Fibrillation. Effective oral anticoagulation according to local routines or a TEE without any finding of intracardial thrombus or signs of thrombogenecity
    boolean
    C0741278 (UMLS CUI [1])
    anticoagulation
    Item
    Clinical indication for cardioversion of Atrial Fibrillation. Effective oral anticoagulation according to local routines or a TEE without any finding of intracardial thrombus or signs of thrombogenecity
    boolean
    C0449867 (UMLS CUI [1])
    TEE
    Item
    Clinical indication for cardioversion of Atrial Fibrillation. Effective oral anticoagulation according to local routines or a TEE without any finding of intracardial thrombus or signs of thrombogenecity
    boolean
    C0206054 (UMLS CUI [1])
    Item Group
    Ausschlusskriterien
    C0680251 (UMLS CUI-1)
    Sinus Node Dysfunction
    Item
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    boolean
    C0428908 (UMLS CUI [1])
    Atrioventricular nodal disease
    Item
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    boolean
    C1841659 (UMLS CUI [1])
    potassium abnormal
    Item
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    boolean
    C0549635 (UMLS CUI [1])
    QTc
    Item
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    boolean
    C0860814 (UMLS CUI [1])
    QRS
    Item
    Clinically significant sinus and/or AV node dysfunction. Serum or plasma potassium <3.8 mmol/L or >5.0 mmol/L. QTc(Bazett) >450 ms. Any QRS duration >150 ms
    boolean
    C1880451 (UMLS CUI [1])

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