0 Evaluaciones

ID

14822

Descripción

Study to Evaluate Efficacy and Tolerance of R-GemOx in DLBCL and MCL; ODM derived from: https://clinicaltrials.gov/show/NCT01562977

Link

https://clinicaltrials.gov/show/NCT01562977

Palabras clave

  1. 29/4/16 29/4/16 -
Subido en

29 de abril de 2016

DOI

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Licencia

Creative Commons BY 4.0

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    Eligibility Aggressive Lymphoma NCT01562977

    Eligibility Aggressive Lymphoma NCT01562977

    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    age ≥ 18 years.
    Descripción

    age

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    dlbcl and mcl diagnosed patients in primary resistance or relapsed not eligible for intensification chemotherapy followed by autologous stem cell transplantation (asct) for age, comorbidity or previous asct.
    Descripción

    Diffuse Large B-Cell Lymphoma

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0079744 (Diffuse Large B-Cell Lymphoma)
    SNOMED
    109969005
    any ipi or ecog, capable of understanding the nature of the trial.
    Descripción

    ecog

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    writtern informed consent.
    Descripción

    informed consent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0021430 (Informed Consent)
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    nursing pregnant or lactation period women, or fertile age adults not using effective contraceptive method.
    Descripción

    pregnant or lactation women

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C2828358 (Lactating (finding))
    UMLS CUI [1,2]
    C0549206 (Patient currently pregnant)
    SNOMED
    77386006
    LOINC
    LA14670-6
    cns lymphoma patients
    Descripción

    Central nervous system lymphoma

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0742472 (undefined)
    patients with severa renal (creatinine> 2,5 unl) or hepatic (bilirrubin or alt/ast> 2,5 unl) impairement not provided by the same disease
    Descripción

    renal or hepatic impairement

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0948807 (Hepatic impairment)
    UMLS CUI [2]
    C0948807 (Hepatic impairment)
    hiv positive patients.
    Descripción

    hiv positive

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0019699 (HIV Seropositivity)
    SNOMED
    165816005
    serious psychiatric diseases patients that could interfere with their skill to understand the study (including alcoholism or drug addiction).
    Descripción

    psychiatric disease

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0004936 (Mental disorders)
    SNOMED
    74732009
    murine proteins or any other component of the medicines of the study hypersensitivity patients.
    Descripción

    murine protein

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1699668 (murine protein)
    patients who have received more than 2 therapeutic previous lines. (for previous asct patients, induction and conditioning for the taph treatment is considered a single line therapy).
    Descripción

    patients who have received more than 2 therapeutic previous lines

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0868551 (Previous exposure to therapeutic or other ionizing radiation)

    Similar models

    Eligibility Aggressive Lymphoma NCT01562977

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    age
    Item
    age ≥ 18 years.
    boolean
    C0001779 (UMLS CUI [1])
    Diffuse Large B-Cell Lymphoma
    Item
    dlbcl and mcl diagnosed patients in primary resistance or relapsed not eligible for intensification chemotherapy followed by autologous stem cell transplantation (asct) for age, comorbidity or previous asct.
    boolean
    C0079744 (UMLS CUI [1])
    ecog
    Item
    any ipi or ecog, capable of understanding the nature of the trial.
    boolean
    C1520224 (UMLS CUI [1])
    informed consent
    Item
    writtern informed consent.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    pregnant or lactation women
    Item
    nursing pregnant or lactation period women, or fertile age adults not using effective contraceptive method.
    boolean
    C2828358 (UMLS CUI [1,1])
    C0549206 (UMLS CUI [1,2])
    Central nervous system lymphoma
    Item
    cns lymphoma patients
    boolean
    C0742472 (UMLS CUI [1])
    renal or hepatic impairement
    Item
    patients with severa renal (creatinine> 2,5 unl) or hepatic (bilirrubin or alt/ast> 2,5 unl) impairement not provided by the same disease
    boolean
    C0948807 (UMLS CUI [1])
    C0948807 (UMLS CUI [2])
    hiv positive
    Item
    hiv positive patients.
    boolean
    C0019699 (UMLS CUI [1])
    psychiatric disease
    Item
    serious psychiatric diseases patients that could interfere with their skill to understand the study (including alcoholism or drug addiction).
    boolean
    C0004936 (UMLS CUI [1])
    murine protein
    Item
    murine proteins or any other component of the medicines of the study hypersensitivity patients.
    boolean
    C1699668 (UMLS CUI [1])
    patients who have received more than 2 therapeutic previous lines
    Item
    patients who have received more than 2 therapeutic previous lines. (for previous asct patients, induction and conditioning for the taph treatment is considered a single line therapy).
    boolean
    C0868551 (UMLS CUI [1])

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