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ID

42247

Descrizione

Ticagrelor is a new, reversible binding, anti-platelet medication. Anti-platelet medications work to prevent the formation of blood clots. Ticagrelor is being developed as a treatment for patients with acute coronary syndrome (ACS). ACS is a term that is used to describe both heart attacks in progress or the imminent threat of a heart attack. ACS is usually caused by the formation of a blood clot in an artery that partially or totally blocks the blood supply to a portion of the heart muscle. Ticagrelor will be compared with clopidogrel to determine which drug, when either is used in conjunction with aspirin, is better at reducing deaths from vascular causes, future heart attacks and/or strokes in patients with ACS. https://clinicaltrials.gov/ct2/show/NCT00391872

collegamento

https://clinicaltrials.gov/ct2/show/NCT00391872

Keywords

  1. 28/11/15 28/11/15 -
  2. 14/04/21 14/04/21 - Ahmed Rafee, MD
  3. 15/04/21 15/04/21 - Ahmed Rafee, MD
Titolare del copyright

AstraZeneca

Caricato su

15 aprile 2021

DOI

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Licenza

Creative Commons BY 4.0

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    Excerpt PLATO Acute coronary Syndrome NCT00391872

    Section Investigational Products

    Investigational product: AZD6140/placebo
    Descrizione

    Investigational product: AZD6140/placebo

    Alias
    UMLS CUI-1
    C1608718
    First dose
    Descrizione

    AZD6140 first dose

    Tipo di dati

    datetime

    Alias
    UMLS CUI [1,1]
    C3173975
    UMLS CUI [1,2]
    C1608718
    Last dose
    Descrizione

    AZD6140 last dose

    Tipo di dati

    datetime

    Alias
    UMLS CUI [1,1]
    C3173975
    UMLS CUI [1,2]
    C1608718
    Investigational product: Clopidogrel/placebo
    Descrizione

    Investigational product: Clopidogrel/placebo

    Alias
    UMLS CUI-1
    C0070166
    First dose
    Descrizione

    Clopidogrel first dose

    Tipo di dati

    datetime

    Alias
    UMLS CUI [1,1]
    C3173975
    UMLS CUI [1,2]
    C0070166
    Last dose
    Descrizione

    Clopidogrel last dose

    Tipo di dati

    datetime

    Alias
    UMLS CUI [1,1]
    C3173975
    UMLS CUI [1,2]
    C0070166
    Additional Dose of Investigational Products
    Descrizione

    Additional Dose of Investigational Products

    Interruption of Investigational Products
    Descrizione

    Interruption of Investigational Products

    Subject Drug Accountability
    Descrizione

    Subject Drug Accountability

    Similar models

    Section Investigational Products

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Investigational product: AZD6140/placebo
    C1608718 (UMLS CUI-1)
    AZD6140 first dose
    Item
    First dose
    datetime
    C3173975 (UMLS CUI [1,1])
    C1608718 (UMLS CUI [1,2])
    AZD6140 last dose
    Item
    Last dose
    datetime
    C3173975 (UMLS CUI [1,1])
    C1608718 (UMLS CUI [1,2])
    Item Group
    Investigational product: Clopidogrel/placebo
    C0070166 (UMLS CUI-1)
    Clopidogrel first dose
    Item
    First dose
    datetime
    C3173975 (UMLS CUI [1,1])
    C0070166 (UMLS CUI [1,2])
    Clopidogrel last dose
    Item
    Last dose
    datetime
    C3173975 (UMLS CUI [1,1])
    C0070166 (UMLS CUI [1,2])
    Item Group
    Additional Dose of Investigational Products
    Item Group
    Interruption of Investigational Products
    Item Group
    Subject Drug Accountability

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