ID

42241

Descrição

The purpose of this trial is to investigate the potential benefits/risks regarding pretreatment with prasugrel in non-ST-elevation myocardial infarction (NSTEMI) participants with elevated troponin scheduled for coronary angiography/percutaneous coronary intervention (PCI). https://clinicaltrials.gov/ct2/show/NCT01015287

Link

https://clinicaltrials.gov/ct2/show/NCT01015287

Palavras-chave

  1. 28/07/2015 28/07/2015 -
  2. 14/04/2021 14/04/2021 - Ahmed Rafee, MD
  3. 14/04/2021 14/04/2021 - Ahmed Rafee, MD
Titular dos direitos

folgt

Transferido a

14 de abril de 2021

DOI

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Licença

Creative Commons BY 4.0

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    Eligibility ACCOAST Acute Coronary Syndrome NCT01015287

    Eligibility criteria

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

    Inclusion Criteria

    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
    Descrição

    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0948089
    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
    Descrição

    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C3537184
    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
    Descrição

    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0523952
    Scheduled for coronary angiography greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization
    Descrição

    Scheduled for coronary angiography greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0085532
    Scheduled for coronary PCI greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization
    Descrição

    Scheduled for coronary PCI greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C1532338
    Must be eligible for treatment with prasugrel
    Descrição

    Must be eligible for treatment with prasugrel

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C1620287
    Must be eligible for treatment with aspirin (ASA)
    Descrição

    Must be eligible for treatment with aspirin (ASA)

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0004057
    Must be eligible for treatment with a glycoprotein IIb/IIIa receptor (GPIIb/IIIa) inhibitor
    Descrição

    Must be eligible for treatment with a glycoprotein IIb/IIIa receptor (GPIIb/IIIa) inhibitor

    Tipo de dados

    text

    Alias
    UMLS CUI-1
    C3640054
    May be on a maintenance dose of clopidogrel 75 mg and must be able to switch to prasugrel
    Descrição

    May be on a maintenance dose of clopidogrel 75 mg and must be able to switch to prasugrel

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0070166
    Must be enrolled at a cardiac catheterization laboratory hospital or at a hospital/ambulance service affiliated with a cardiac catheterization laboratory hospital
    Descrição

    Must be enrolled at a cardiac catheterization laboratory hospital or at a hospital/ambulance service affiliated with a cardiac catheterization laboratory hospital

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0019994
    UMLS CUI [1,2]
    C0018795
    Exclusion Criteria
    Descrição

    Exclusion Criteria

    Present with ST-segment elevation myocardial infarction (STEMI) at the time of entry or randomization
    Descrição

    Present with ST-segment elevation myocardial infarction (STEMI) at the time of entry or randomization

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C1536220
    Have cardiogenic shock
    Descrição

    Have cardiogenic shock

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0036980
    Have refractory ventricular arrhythmias
    Descrição

    Have refractory ventricular arrhythmias

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0085612
    Have New York Heart Association (NYHA) Class IV congestive heart failure (CHF)
    Descrição

    Have New York Heart Association (NYHA) Class IV congestive heart failure (CHF)

    Tipo de dados

    text

    Alias
    UMLS CUI-1
    C1319796
    UMLS CUI-2
    C0018802
    Have had cardiac arrest within 1 week of entry or randomization into the study
    Descrição

    Have had cardiac arrest within 1 week of entry or randomization into the study

    Tipo de dados

    boolean

    Alias
    UMLS CUI-1
    C0018790

    Similar models

    Eligibility criteria

    1. StudyEvent: ODM
      1. Eligibility criteria
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    Inclusion Criteria
    Acute coronary syndrome
    Item
    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
    boolean
    C0948089 (UMLS CUI-1)
    NSTEMI
    Item
    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
    boolean
    C3537184 (UMLS CUI-1)
    Troponin
    Item
    Have acute coronary syndrome consisting of non-ST-segment elevation with elevated troponin
    boolean
    C0523952 (UMLS CUI-1)
    Coronary angiography
    Item
    Scheduled for coronary angiography greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization
    boolean
    C0085532 (UMLS CUI-1)
    PCI
    Item
    Scheduled for coronary PCI greater than or equal to 2 and less than 24 hours from time of planned randomization, but no more than 48 hours from randomization
    boolean
    C1532338 (UMLS CUI-1)
    Prasugrel
    Item
    Must be eligible for treatment with prasugrel
    boolean
    C1620287 (UMLS CUI-1)
    Aspirin
    Item
    Must be eligible for treatment with aspirin (ASA)
    boolean
    C0004057 (UMLS CUI-1)
    GP IIb/IIIa antagonist
    Item
    Must be eligible for treatment with a glycoprotein IIb/IIIa receptor (GPIIb/IIIa) inhibitor
    text
    C3640054 (UMLS CUI-1)
    Clopidogrel
    Item
    May be on a maintenance dose of clopidogrel 75 mg and must be able to switch to prasugrel
    boolean
    C0070166 (UMLS CUI-1)
    Cardiac catheterization laboratory
    Item
    Must be enrolled at a cardiac catheterization laboratory hospital or at a hospital/ambulance service affiliated with a cardiac catheterization laboratory hospital
    boolean
    C0019994 (UMLS CUI [1,1])
    C0018795 (UMLS CUI [1,2])
    Item Group
    Exclusion Criteria
    STEMI
    Item
    Present with ST-segment elevation myocardial infarction (STEMI) at the time of entry or randomization
    boolean
    C1536220 (UMLS CUI-1)
    Cardiogenic shock
    Item
    Have cardiogenic shock
    boolean
    C0036980 (UMLS CUI-1)
    Ventricular arrhythmia
    Item
    Have refractory ventricular arrhythmias
    boolean
    C0085612 (UMLS CUI-1)
    Congestive heart failure
    Item
    Have New York Heart Association (NYHA) Class IV congestive heart failure (CHF)
    text
    C1319796 (UMLS CUI-1)
    C0018802 (UMLS CUI-2)
    Cardiac arrest
    Item
    Have had cardiac arrest within 1 week of entry or randomization into the study
    boolean
    C0018790 (UMLS CUI-1)

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