0 Ratings

ID

34353

Description

Autologous Bone Marrow Mononuclear Cells in the Combined Treatment of Coronary Heart Disease; ODM derived from: https://clinicaltrials.gov/show/NCT02059512

Link

https://clinicaltrials.gov/show/NCT02059512

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

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License

Creative Commons BY 4.0

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    Eligibility Ischemic Heart Disease NCT02059512

    Eligibility Ischemic Heart Disease NCT02059512

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    men and women from 18 to 80 years
    Description

    ID.1

    Data type

    boolean

    patients with angina pectoris iii-iv functional class
    Description

    ID.2

    Data type

    boolean

    patients signed informed consent
    Description

    ID.3

    Data type

    boolean

    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    intolerance of heparin and hes.
    Description

    ID.4

    Data type

    boolean

    hypothyroidism and hyperthyroidism.
    Description

    ID.5

    Data type

    boolean

    associated pathology with a projected lifespan limitation to 3 years.
    Description

    ID.6

    Data type

    boolean

    infection diseases
    Description

    ID.7

    Data type

    boolean

    simultaneous participation in another study.
    Description

    ID.8

    Data type

    boolean

    pregnancy.
    Description

    ID.9

    Data type

    boolean

    severe mental disorder.
    Description

    ID.10

    Data type

    boolean

    refusal of a patient to participate in the study.
    Description

    ID.11

    Data type

    boolean

    Similar models

    Eligibility Ischemic Heart Disease NCT02059512

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    ID.1
    Item
    men and women from 18 to 80 years
    boolean
    ID.2
    Item
    patients with angina pectoris iii-iv functional class
    boolean
    ID.3
    Item
    patients signed informed consent
    boolean
    Item Group
    C0680251 (UMLS CUI)
    ID.4
    Item
    intolerance of heparin and hes.
    boolean
    ID.5
    Item
    hypothyroidism and hyperthyroidism.
    boolean
    ID.6
    Item
    associated pathology with a projected lifespan limitation to 3 years.
    boolean
    ID.7
    Item
    infection diseases
    boolean
    ID.8
    Item
    simultaneous participation in another study.
    boolean
    ID.9
    Item
    pregnancy.
    boolean
    ID.10
    Item
    severe mental disorder.
    boolean
    ID.11
    Item
    refusal of a patient to participate in the study.
    boolean

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