0 Evaluaciones
ID

16732

Descripción

Weekly Topotecan in Patients Treated for Metastatic Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193167

Link

https://clinicaltrials.gov/show/NCT00193167

Palabras clave

Versiones (1)
  1. 3/8/16 3/8/16 -
Subido en

3 de agosto de 2016

DOI

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Licencia

Creative Commons BY 4.0
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    Eligibility Colon Cancer NCT00193167

    Inglés

    Eligibility Colon Cancer NCT00193167

    1 formularios  
    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    to be included in this study, you must meet the following criteria:
    Descripción

    criteria Fulfill

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0243161
    UMLS CUI [1,2]
    C1550543
    metastatic colorectal cancer
    Descripción

    Colorectal cancer metastatic

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0948380
    one previous chemotherapy for metastatic disease
    Descripción

    Prior Chemotherapy Quantity Neoplasm Metastasis

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1514457
    UMLS CUI [1,2]
    C1265611
    UMLS CUI [1,3]
    C0027627
    measurable or evaluable disease
    Descripción

    Measurable Disease | Evaluable Disease

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1513041
    UMLS CUI [2]
    C1516986
    able to perform activities of daily living with assistance
    Descripción

    Performance of activities of daily living Assisted Ability

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1821398
    UMLS CUI [1,2]
    C1269765
    UMLS CUI [1,3]
    C0085732
    adequate bone marrow, liver, and kidney function
    Descripción

    Bone Marrow function | Liver function | Renal function

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0005953
    UMLS CUI [1,2]
    C0031843
    UMLS CUI [2]
    C0232741
    UMLS CUI [3]
    C0232804
    all patients must give written informed consent prior to study entry.
    Descripción

    Informed consent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    you cannot participate in this study if any of the following apply to you:
    Descripción

    Study Subject Participation Status

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    brain or meningeal involvement
    Descripción

    Brain Involvement | Meninges Involvement

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0006104
    UMLS CUI [1,2]
    C1314939
    UMLS CUI [2,1]
    C0025285
    UMLS CUI [2,2]
    C1314939
    serious active infection or underlying medical conditions
    Descripción

    Communicable Diseases Serious | medical condition Serious

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0009450
    UMLS CUI [1,2]
    C0205404
    UMLS CUI [2,1]
    C3843040
    UMLS CUI [2,2]
    C0205404
    other active neoplasms are ineligible
    Descripción

    Neoplasms

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0027651
    pregnant or lactating
    Descripción

    Pregnancy | Breast Feeding

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
    Descripción

    Study Subject Participation Status

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2348568
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    Similar models

    Eligibility Colon Cancer NCT00193167

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    criteria Fulfill
    Item
    to be included in this study, you must meet the following criteria:
    boolean
    C0243161 (UMLS CUI [1,1])
    C1550543 (UMLS CUI [1,2])
    Colorectal cancer metastatic
    Item
    metastatic colorectal cancer
    boolean
    C0948380 (UMLS CUI [1])
    Prior Chemotherapy Quantity Neoplasm Metastasis
    Item
    one previous chemotherapy for metastatic disease
    boolean
    C1514457 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    C0027627 (UMLS CUI [1,3])
    Measurable Disease | Evaluable Disease
    Item
    measurable or evaluable disease
    boolean
    C1513041 (UMLS CUI [1])
    C1516986 (UMLS CUI [2])
    Performance of activities of daily living Assisted Ability
    Item
    able to perform activities of daily living with assistance
    boolean
    C1821398 (UMLS CUI [1,1])
    C1269765 (UMLS CUI [1,2])
    C0085732 (UMLS CUI [1,3])
    Bone Marrow function | Liver function | Renal function
    Item
    adequate bone marrow, liver, and kidney function
    boolean
    C0005953 (UMLS CUI [1,1])
    C0031843 (UMLS CUI [1,2])
    C0232741 (UMLS CUI [2])
    C0232804 (UMLS CUI [3])
    Informed consent
    Item
    all patients must give written informed consent prior to study entry.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Study Subject Participation Status
    Item
    you cannot participate in this study if any of the following apply to you:
    boolean
    C2348568 (UMLS CUI [1])
    Brain Involvement | Meninges Involvement
    Item
    brain or meningeal involvement
    boolean
    C0006104 (UMLS CUI [1,1])
    C1314939 (UMLS CUI [1,2])
    C0025285 (UMLS CUI [2,1])
    C1314939 (UMLS CUI [2,2])
    Communicable Diseases Serious | medical condition Serious
    Item
    serious active infection or underlying medical conditions
    boolean
    C0009450 (UMLS CUI [1,1])
    C0205404 (UMLS CUI [1,2])
    C3843040 (UMLS CUI [2,1])
    C0205404 (UMLS CUI [2,2])
    Neoplasms
    Item
    other active neoplasms are ineligible
    boolean
    C0027651 (UMLS CUI [1])
    Pregnancy | Breast Feeding
    Item
    pregnant or lactating
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Study Subject Participation Status
    Item
    please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
    boolean
    C2348568 (UMLS CUI [1])
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