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ID

34353

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02059512

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility Ischemic Heart Disease NCT02059512

    Eligibility Ischemic Heart Disease NCT02059512

    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

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

    ID.1

    Datatyp

    boolean

    patients with angina pectoris iii-iv functional class
    Beskrivning

    ID.2

    Datatyp

    boolean

    patients signed informed consent
    Beskrivning

    ID.3

    Datatyp

    boolean

    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

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

    ID.4

    Datatyp

    boolean

    hypothyroidism and hyperthyroidism.
    Beskrivning

    ID.5

    Datatyp

    boolean

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

    ID.6

    Datatyp

    boolean

    infection diseases
    Beskrivning

    ID.7

    Datatyp

    boolean

    simultaneous participation in another study.
    Beskrivning

    ID.8

    Datatyp

    boolean

    pregnancy.
    Beskrivning

    ID.9

    Datatyp

    boolean

    severe mental disorder.
    Beskrivning

    ID.10

    Datatyp

    boolean

    refusal of a patient to participate in the study.
    Beskrivning

    ID.11

    Datatyp

    boolean

    Similar models

    Eligibility Ischemic Heart Disease NCT02059512

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    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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