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ID

14822

Beschreibung

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

Stichworte

  1. 29.04.16 29.04.16 -
Hochgeladen am

29. April 2016

DOI

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Lizenz

Creative Commons BY 4.0

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    Eligibility Aggressive Lymphoma NCT01562977

    Eligibility Aggressive Lymphoma NCT01562977

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

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

    age

    Datentyp

    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.
    Beschreibung

    Diffuse Large B-Cell Lymphoma

    Datentyp

    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.
    Beschreibung

    ecog

    Datentyp

    boolean

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

    informed consent

    Datentyp

    boolean

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

    Exclusion Criteria

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

    pregnant or lactation women

    Datentyp

    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
    Beschreibung

    Central nervous system lymphoma

    Datentyp

    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
    Beschreibung

    renal or hepatic impairement

    Datentyp

    boolean

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

    hiv positive

    Datentyp

    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).
    Beschreibung

    psychiatric disease

    Datentyp

    boolean

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

    murine protein

    Datentyp

    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).
    Beschreibung

    patients who have received more than 2 therapeutic previous lines

    Datentyp

    boolean

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

    Ähnliche Modelle

    Eligibility Aggressive Lymphoma NCT01562977

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    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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