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ID

43958

Descrizione

A Study of IL-12 in Patients With Acute Myelogenous Leukemia (AML); ODM derived from: https://clinicaltrials.gov/show/NCT02483312

collegamento

https://clinicaltrials.gov/show/NCT02483312

Keywords

  1. 01/04/16 01/04/16 -
  2. 20/09/21 20/09/21 -
Caricato su

20 settembre 2021

DOI

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Licenza

Creative Commons BY 4.0

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    Eligibility Acute Myeloid Leukemia NCT02483312

    Eligibility Acute Myeloid Leukemia NCT02483312

    Inclusion Criteria
    Descrizione

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patient with aml and >=18 years of age.
    Descrizione

    AML

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0023467
    Patient agrees to participate in the study and signs the informed consent
    Descrizione

    Informed Consent

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    viably frozen cells from the time of diagnosis or relapse are available
    Descrizione

    Peripheral blood mononuclear cell

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1321301
    first complete remission and have high risk features of relapse.
    Descrizione

    In complete remission

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0677874
    less than 10% blast cells in the bone marrow following induction or re-induction therapy and not desiring further intensive treatment.
    Descrizione

    Blast Cell

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0368761
    acceptable creatinine, ast, alp, bilirubin
    Descrizione

    Creatinine

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0010294
    agree to use contraception
    Descrizione

    Contraceptive methods

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0700589
    not pregnant
    Descrizione

    Not pregnant

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0232973
    able to comply with study procedures
    Descrizione

    comply with study procedures

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0525058
    Exclusion Criteria
    Descrizione

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    ecog performance status <2
    Descrizione

    ECOG performance status

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    known persistent infection
    Descrizione

    Persistent infection

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C1264606
    known cns disease
    Descrizione

    cns disease

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0007682
    greater than 10% blasts in the bone marrow or circulating blast cells
    Descrizione

    Blast Cell

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0368761
    life expectancy < 2 months
    Descrizione

    Life Expectancy

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0023671
    receiving any chemotherapy, corticosteroids, cox2 inhibitors or any non-drug therapies with the intent of altering the immune response or kill leukemic cells within one week prior to infusion of il-12 -infected cells.
    Descrizione

    Leukemic Cells

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0020964
    UMLS CUI [2]
    C3890400

    Similar models

    Eligibility Acute Myeloid Leukemia NCT02483312

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    C1512693 (UMLS CUI)
    AML
    Item
    patient with aml and >=18 years of age.
    boolean
    C0023467 (UMLS CUI [1])
    Informed Consent
    Item
    Patient agrees to participate in the study and signs the informed consent
    boolean
    C0021430 (UMLS CUI [1])
    Peripheral blood mononuclear cell
    Item
    viably frozen cells from the time of diagnosis or relapse are available
    boolean
    C1321301 (UMLS CUI [1])
    In complete remission
    Item
    first complete remission and have high risk features of relapse.
    boolean
    C0677874 (UMLS CUI [1])
    Blast Cell
    Item
    less than 10% blast cells in the bone marrow following induction or re-induction therapy and not desiring further intensive treatment.
    boolean
    C0368761 (UMLS CUI [1])
    Creatinine
    Item
    acceptable creatinine, ast, alp, bilirubin
    boolean
    C0010294 (UMLS CUI [1])
    Contraceptive methods
    Item
    agree to use contraception
    boolean
    C0700589 (UMLS CUI [1])
    Not pregnant
    Item
    not pregnant
    boolean
    C0232973 (UMLS CUI [1])
    comply with study procedures
    Item
    able to comply with study procedures
    boolean
    C0525058 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    ECOG performance status
    Item
    ecog performance status <2
    boolean
    C1520224 (UMLS CUI [1])
    Persistent infection
    Item
    known persistent infection
    boolean
    C1264606 (UMLS CUI [1])
    cns disease
    Item
    known cns disease
    boolean
    C0007682 (UMLS CUI [1])
    Blast Cell
    Item
    greater than 10% blasts in the bone marrow or circulating blast cells
    boolean
    C0368761 (UMLS CUI [1])
    Life Expectancy
    Item
    life expectancy < 2 months
    boolean
    C0023671 (UMLS CUI [1])
    Leukemic Cells
    Item
    receiving any chemotherapy, corticosteroids, cox2 inhibitors or any non-drug therapies with the intent of altering the immune response or kill leukemic cells within one week prior to infusion of il-12 -infected cells.
    boolean
    C0020964 (UMLS CUI [1])
    C3890400 (UMLS CUI [2])

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