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ID

11709

Beskrivning

The purpose of this study is to evaluate the safety of rivaroxaban in patients with recent acute coronary syndrome (ACS) and to assess the ability of rivaroxaban to reduce the occurrence of death, myocardial infarction (heart attack), repeat myocardial infarctions, stroke, and ischemia (inadequate blood supply to a local area) in patients with recent ACS. https://clinicaltrials.gov/ct2/show/NCT00402597

Länk

https://clinicaltrials.gov/ct2/show/NCT00402597

Nyckelord

  1. 2015-07-28 2015-07-28 -
Uppladdad den

28 juli 2015

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility ATLAS ACS TIMI 46 Acute Coronary Syndrome NCT00402597

    Eligibility criteria

    1. StudyEvent: ODM
      1. Eligibility criteria
    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    Have symptoms suggestive of ACS that lasted at least 10 minutes at rest occurring within 7 days of randomization
    Beskrivning

    Have symptoms suggestive of ACS that lasted at least 10 minutes at rest occurring within 7 days of randomization

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0948089 (Acute Coronary Syndrome)
    SNOMED
    394659003
    diagnosis of ST-elevation myocardial infarction
    Beskrivning

    diagnosis of ST-elevation myocardial infarction

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C1536220 (ST segment elevation myocardial infarction)
    diagnosis non-ST elevation myocardial infarction
    Beskrivning

    diagnosis non-ST elevation myocardial infarction

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C3537184 (Non-ST Elevation Myocardial Infarction by ECG Finding)
    diagnosis of unstable angina
    Beskrivning

    diagnosis of unstable angina

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0002965 (Angina, Unstable)
    SNOMED
    4557003
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Active bleeding
    Beskrivning

    Active bleeding

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0019080 (Hemorrhage)
    SNOMED
    50960005
    LOINC
    LA7418-2
    risk of bleeding
    Beskrivning

    risk of bleeding

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C3251812 (Bleeding risk)
    LOINC
    LP209013-4
    intracranial hemorrhage
    Beskrivning

    intracranial hemorrhage

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0151699 (Intracranial Hemorrhage)
    SNOMED
    1386000
    anticoagulant therapy
    Beskrivning

    anticoagulant therapy

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0150457 (Anticoagulant therapy)
    SNOMED
    182764009
    LOINC
    LA28199-0
    Significantly impaired renal function
    Beskrivning

    Significantly impaired renal function

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0035078 (Kidney Failure)
    SNOMED
    723188008
    Significantly impaired hepatic function
    Beskrivning

    Significantly impaired hepatic function

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0085605 (Liver Failure)
    SNOMED
    59927004
    cardiogenic shock
    Beskrivning

    cardiogenic shock

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0036980 (Shock, Cardiogenic)
    SNOMED
    89138009
    ventricular arrhythmias
    Beskrivning

    ventricular arrhythmias

    Datatyp

    boolean

    Alias
    UMLS CUI-1
    C0085612 (Ventricular arrhythmia)
    SNOMED
    44103008

    Similar models

    Eligibility criteria

    1. StudyEvent: ODM
      1. Eligibility criteria
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Inclusion Criteria
    Acute coronary syndrome
    Item
    Have symptoms suggestive of ACS that lasted at least 10 minutes at rest occurring within 7 days of randomization
    boolean
    C0948089 (UMLS CUI-1)
    STEMI
    Item
    diagnosis of ST-elevation myocardial infarction
    boolean
    C1536220 (UMLS CUI-1)
    NSTEMI
    Item
    diagnosis non-ST elevation myocardial infarction
    boolean
    C3537184 (UMLS CUI-1)
    Unstable angina
    Item
    diagnosis of unstable angina
    boolean
    C0002965 (UMLS CUI-1)
    Item Group
    Exclusion Criteria
    Hemorrhage
    Item
    Active bleeding
    boolean
    C0019080 (UMLS CUI-1)
    Bleeding risk
    Item
    risk of bleeding
    boolean
    C3251812 (UMLS CUI-1)
    intracranial hemorrhage
    Item
    intracranial hemorrhage
    boolean
    C0151699 (UMLS CUI-1)
    anticoagulant therapy
    Item
    anticoagulant therapy
    boolean
    C0150457 (UMLS CUI-1)
    Kidney failure
    Item
    Significantly impaired renal function
    boolean
    C0035078 (UMLS CUI-1)
    Liver failure
    Item
    Significantly impaired hepatic function
    boolean
    C0085605 (UMLS CUI-1)
    cardiogenic shock
    Item
    cardiogenic shock
    boolean
    C0036980 (UMLS CUI-1)
    ventricular arrhythmia
    Item
    ventricular arrhythmias
    boolean
    C0085612 (UMLS CUI-1)

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