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ID

12617

Beskrivning

EPOCH Chemotherapy +/- IL-12 for Previously Untreated and EPOCH Plus Rituximab for Previously Treated Patients With AIDS-Associated Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00001563

Länk

https://clinicaltrials.gov/show/NCT00001563

Nyckelord

  1. 2015-12-06 2015-12-06 -
Uppladdad den

6 december 2015

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility AIDS Related Lymphoma NCT00001563

    Eligibility AIDS Related Lymphoma NCT00001563

    Criteria
    Beskrivning

    Criteria

    aggressive cd20 + nhl confirmed by pathology, dcs.
    Beskrivning

    aggressive cd20 + nhl confirmed by pathology, dcs.

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0852469
    UMLS CUI [1,2]
    C0882818
    UMLS CUI [1,3]
    C0679557
    hiv + serology.
    Beskrivning

    HIV

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0019699
    all stages (i-iv) of disease.
    Beskrivning

    all stages (i-iv) of disease.

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0019699
    nhl previously treated with up to two chemotherapy regimens and evaluable disease.
    Beskrivning

    nhl previously treated with up to two chemotherapy regimens and evaluable disease.

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0852469
    UMLS CUI [1,2]
    C1514457
    UMLS CUI [1,3]
    C1516986
    age greater than or equal to 18 years.
    Beskrivning

    Age

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    laboratory test: (abnormalities are allowed if due to organ involvement by lymphoma).
    Beskrivning

    ID.6

    Datatyp

    boolean

    creatinine less than or equal to 1.7.
    Beskrivning

    creatinine levels

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1561535
    bilirubin must be less than 2.0 mg/dl, or total bilirubin less than or equal to 3.7 mg/dl with direct fraction less than or equal to 0.2 mg/dl and indirect fraction of less than or equal 3.5 mg/dl in patients for whom these abnormalities are felt to be due to protease inhibitor therapy.
    Beskrivning

    Bilirubin levels

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1557209
    ast and alt less than or equal to 3 times uln (ast and alt less than or equal to 6 times uln for patients on hyperalimentation for whom these abnormalities are felt to be due to the hyperalimentation).
    Beskrivning

    AST and ALT levels

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0201836
    UMLS CUI [2]
    C0201899
    anc greater than or equal 1000/mm(3).
    Beskrivning

    Absolute neutrophil count

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0948762
    platelets must be greater than or equal to 75,000/mm(3) (patients with itp platelets greater than or equal to 30,000/mm(3).
    Beskrivning

    Platelet count

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0005821
    signed informed consent and durable power of attorney.
    Beskrivning

    signed informed consent and durable power of attorney.

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    Pregnancy or nursing
    Beskrivning

    Pregnancy or nursing.

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0549206
    UMLS CUI [1,2]
    C0006147
    history of clinical heart failure or symptomatic ischemic heart disease.
    Beskrivning

    history of clinical heart failure or symptomatic ischemic heart disease.

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C2004062
    UMLS CUI [1,2]
    C0018801
    UMLS CUI [1,3]
    C0151744
    serious underlying medical condition or infection other than hiv that would contraindicate epoch.
    Beskrivning

    serious underlying medical condition or infection other than hiv that would contraindicate epoch.

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0009488
    UMLS CUI [1,2]
    C1301624
    UMLS CUI [1,3]
    C2946699
    concurrent anti-retroviral therapy during epoch therapy.
    Beskrivning

    concurrent anti-retroviral therapy during epoch therapy.

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0205420
    UMLS CUI [1,2]
    C1963724
    primary cns lymphoma.
    Beskrivning

    primary cns lymphoma.

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0280803

    Similar models

    Eligibility AIDS Related Lymphoma NCT00001563

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    aggressive cd20 + nhl confirmed by pathology, dcs.
    Item
    aggressive cd20 + nhl confirmed by pathology, dcs.
    text
    C0852469 (UMLS CUI [1,1])
    C0882818 (UMLS CUI [1,2])
    C0679557 (UMLS CUI [1,3])
    HIV
    Item
    hiv + serology.
    boolean
    C0019699 (UMLS CUI [1])
    all stages (i-iv) of disease.
    Item
    all stages (i-iv) of disease.
    boolean
    C0019699 (UMLS CUI [1])
    nhl previously treated with up to two chemotherapy regimens and evaluable disease.
    Item
    nhl previously treated with up to two chemotherapy regimens and evaluable disease.
    boolean
    C0852469 (UMLS CUI [1,1])
    C1514457 (UMLS CUI [1,2])
    C1516986 (UMLS CUI [1,3])
    Age
    Item
    age greater than or equal to 18 years.
    boolean
    C0001779 (UMLS CUI [1])
    ID.6
    Item
    laboratory test: (abnormalities are allowed if due to organ involvement by lymphoma).
    boolean
    creatinine levels
    Item
    creatinine less than or equal to 1.7.
    boolean
    C1561535 (UMLS CUI [1])
    Bilirubin levels
    Item
    bilirubin must be less than 2.0 mg/dl, or total bilirubin less than or equal to 3.7 mg/dl with direct fraction less than or equal to 0.2 mg/dl and indirect fraction of less than or equal 3.5 mg/dl in patients for whom these abnormalities are felt to be due to protease inhibitor therapy.
    boolean
    C1557209 (UMLS CUI [1])
    AST and ALT levels
    Item
    ast and alt less than or equal to 3 times uln (ast and alt less than or equal to 6 times uln for patients on hyperalimentation for whom these abnormalities are felt to be due to the hyperalimentation).
    boolean
    C0201836 (UMLS CUI [1])
    C0201899 (UMLS CUI [2])
    Absolute neutrophil count
    Item
    anc greater than or equal 1000/mm(3).
    boolean
    C0948762 (UMLS CUI [1])
    Platelet count
    Item
    platelets must be greater than or equal to 75,000/mm(3) (patients with itp platelets greater than or equal to 30,000/mm(3).
    boolean
    C0005821 (UMLS CUI [1])
    signed informed consent and durable power of attorney.
    Item
    signed informed consent and durable power of attorney.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Pregnancy or nursing.
    Item
    Pregnancy or nursing
    boolean
    C0549206 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])
    history of clinical heart failure or symptomatic ischemic heart disease.
    Item
    history of clinical heart failure or symptomatic ischemic heart disease.
    boolean
    C2004062 (UMLS CUI [1,1])
    C0018801 (UMLS CUI [1,2])
    C0151744 (UMLS CUI [1,3])
    serious underlying medical condition or infection other than hiv that would contraindicate epoch.
    Item
    serious underlying medical condition or infection other than hiv that would contraindicate epoch.
    boolean
    C0009488 (UMLS CUI [1,1])
    C1301624 (UMLS CUI [1,2])
    C2946699 (UMLS CUI [1,3])
    concurrent anti-retroviral therapy during epoch therapy.
    Item
    concurrent anti-retroviral therapy during epoch therapy.
    boolean
    C0205420 (UMLS CUI [1,1])
    C1963724 (UMLS CUI [1,2])
    primary cns lymphoma.
    Item
    primary cns lymphoma.
    boolean
    C0280803 (UMLS CUI [1])

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