ID

12903

Description

The Atrial High Rate Episodes in Pacemaker Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00627328

Lien

https://clinicaltrials.gov/show/NCT00627328

Mots-clés

  1. 05/01/2016 05/01/2016 -
Téléchargé le

5 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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    Eligibility Arrhythmia NCT00627328

    Eligibility Arrhythmia NCT00627328

    1. StudyEvent: Eligibility
      1. Eligibility Arrhythmia NCT00627328
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patients undergoing a medtronic kappa dr 700 or medtronic kappa 900 dr implant, for approved indications
    Description

    pacemaker

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0030163
    no previous history of pacemaker implantation
    Description

    pacemaker

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0030163
    patients 50 years of age or older
    Description

    age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    patients with a history of atrial tachyarrhythmias (primary arm of study)
    Description

    comorbidity

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    patients with medical conditions that would limit study participation
    Description

    comorbidity

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    patients inaccessible for follow-up at the study center
    Description

    follow-up

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1522577
    patients incapable of providing informed consent
    Description

    informed consent

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    patients with nyha classification of iv
    Description

    nyha

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1275491
    patients with a history of neurocardiogenic syncope, long qt syndrome, or hypertrophic obstructive cardiomyopathy (hocm)
    Description

    comorbidity

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    patients taking sotalol or amiodorone
    Description

    sotalol, amiodarone

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0037707
    UMLS CUI [2]
    C0002598
    patients with a history of a prior icd or pacemaker implantation.
    Description

    icd, pacemaker

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0162589
    UMLS CUI [2]
    C0030163

    Similar models

    Eligibility Arrhythmia NCT00627328

    1. StudyEvent: Eligibility
      1. Eligibility Arrhythmia NCT00627328
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    pacemaker
    Item
    patients undergoing a medtronic kappa dr 700 or medtronic kappa 900 dr implant, for approved indications
    boolean
    C0030163 (UMLS CUI [1])
    pacemaker
    Item
    no previous history of pacemaker implantation
    boolean
    C0030163 (UMLS CUI [1])
    age
    Item
    patients 50 years of age or older
    boolean
    C0001779 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    comorbidity
    Item
    patients with a history of atrial tachyarrhythmias (primary arm of study)
    boolean
    C0009488 (UMLS CUI [1])
    comorbidity
    Item
    patients with medical conditions that would limit study participation
    boolean
    C1321605 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    follow-up
    Item
    patients inaccessible for follow-up at the study center
    boolean
    C1522577 (UMLS CUI [1])
    informed consent
    Item
    patients incapable of providing informed consent
    boolean
    C0021430 (UMLS CUI [1])
    nyha
    Item
    patients with nyha classification of iv
    boolean
    C1275491 (UMLS CUI [1])
    comorbidity
    Item
    patients with a history of neurocardiogenic syncope, long qt syndrome, or hypertrophic obstructive cardiomyopathy (hocm)
    boolean
    C0009488 (UMLS CUI [1])
    sotalol, amiodarone
    Item
    patients taking sotalol or amiodorone
    boolean
    C0037707 (UMLS CUI [1])
    C0002598 (UMLS CUI [2])
    icd, pacemaker
    Item
    patients with a history of a prior icd or pacemaker implantation.
    boolean
    C0162589 (UMLS CUI [1])
    C0030163 (UMLS CUI [2])

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