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ID

34417

Beschrijving

Non-isotope Based Imaging Modalities vs Technetium-99m Single-Photon Emission Computed Tomography(99mTcSPECT); ODM derived from: https://clinicaltrials.gov/show/NCT01972360

Link

https://clinicaltrials.gov/show/NCT01972360

Trefwoorden

  1. 17-01-19 17-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

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    Eligibility Myocardial Ischemia NCT01972360

    Eligibility Myocardial Ischemia NCT01972360

    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    clinically indicated request for spect
    Beschrijving

    ID.1

    Datatype

    boolean

    ability to undergo at least one of three non-nuclear imaging tests; cmr, ct or stress echocardiography
    Beschrijving

    ID.2

    Datatype

    boolean

    history of recent symptoms suggestive of myocardial ischemia
    Beschrijving

    ID.3

    Datatype

    boolean

    high risk for ischemic cardiovascular events
    Beschrijving

    ID.4

    Datatype

    boolean

    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    severely reduced systolic function (lv ejection fraction less than 35%)
    Beschrijving

    ID.5

    Datatype

    boolean

    recent (less than 3 days) acute coronary syndrome including acute myocardial infarction
    Beschrijving

    ID.6

    Datatype

    boolean

    contraindications to dipyridamole spect including : i)severe reactive airway disease; ii) less than 3 days post myocardial infarction - acute coronary syndrome (mi-acs); iii) high-grade atrioventricular block (av block); iv)allergy to dipyridamole or theophylline; v) caffeine within 12 hours; vi) theophylline use within 48 hours; vii) severe claustrophobia; or viii) women who may be pregnant
    Beschrijving

    ID.7

    Datatype

    boolean

    kidney dysfunction (i.e estimated glomerular filtration rate (egfr) less than 45)
    Beschrijving

    ID.8

    Datatype

    boolean

    use of investigational drug or device within 30 days of screening visit
    Beschrijving

    ID.9

    Datatype

    boolean

    Similar models

    Eligibility Myocardial Ischemia NCT01972360

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    ID.1
    Item
    clinically indicated request for spect
    boolean
    ID.2
    Item
    ability to undergo at least one of three non-nuclear imaging tests; cmr, ct or stress echocardiography
    boolean
    ID.3
    Item
    history of recent symptoms suggestive of myocardial ischemia
    boolean
    ID.4
    Item
    high risk for ischemic cardiovascular events
    boolean
    Item Group
    C0680251 (UMLS CUI)
    ID.5
    Item
    severely reduced systolic function (lv ejection fraction less than 35%)
    boolean
    ID.6
    Item
    recent (less than 3 days) acute coronary syndrome including acute myocardial infarction
    boolean
    ID.7
    Item
    contraindications to dipyridamole spect including : i)severe reactive airway disease; ii) less than 3 days post myocardial infarction - acute coronary syndrome (mi-acs); iii) high-grade atrioventricular block (av block); iv)allergy to dipyridamole or theophylline; v) caffeine within 12 hours; vi) theophylline use within 48 hours; vii) severe claustrophobia; or viii) women who may be pregnant
    boolean
    ID.8
    Item
    kidney dysfunction (i.e estimated glomerular filtration rate (egfr) less than 45)
    boolean
    ID.9
    Item
    use of investigational drug or device within 30 days of screening visit
    boolean

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