0 Evaluaciones
ID

12862

Descripción

A Clinical Trial of Vorinostat (MK0683, SAHA) in Combination With FDA Approved Cancer Drugs in Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)(0683-056); ODM derived from: https://clinicaltrials.gov/show/NCT00473889

Link

https://clinicaltrials.gov/show/NCT00473889

Palabras clave

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

3 de enero de 2016

DOI

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Licencia

Creative Commons BY 4.0
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    Eligibility Stage IIIB or IV Non-Small Cell Lung Cancer NCT00473889

    Inglés

    Eligibility Stage IIIB or IV Non-Small Cell Lung Cancer NCT00473889

    1 formularios  
    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    males and females at least 18 years of age who have confirmed diagnosis of non-small cell lung cancer
    Descripción

    age; non-small cell lung cancer

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    UMLS CUI [2]
    C0007131 (Non-Small Cell Lung Carcinoma)
    SNOMED
    254637007
    patients with no systemic prior systemic treatment for lung cancer except patients at least 12 months from prior adjuvant therapy
    Descripción

    therapy systemic lung cancer

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0087111 (Therapeutic procedure)
    SNOMED
    277132007
    LOINC
    LP21090-3
    UMLS CUI [1,2]
    C0205373 (Systemic)
    SNOMED
    31099001
    UMLS CUI [1,3]
    C0242379 (Malignant neoplasm of lung)
    SNOMED
    363358000
    adequate bone marrow,kidney and liver function
    Descripción

    organ function adequate; liver function

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0678852 (body system or organ function)
    UMLS CUI [1,2]
    C0205411 (Adequate)
    SNOMED
    88323005
    LOINC
    LA8913-1
    UMLS CUI [2]
    C0232741 (Liver function)
    SNOMED
    79036002
    LOINC
    LP31397-0
    must be recovered and at least 4 weeks from major surgery or radiation
    Descripción

    major surgery; radiation

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0679637 (major surgery)
    UMLS CUI [2]
    C0851346 (Radiation)
    SNOMED
    82107009
    LOINC
    MTHU026213
    ecog (eastern cooperative oncology group) performance status of 0 or 1
    Descripción

    ecog

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    men and women must agree to use birth control during the study
    Descripción

    contraception status

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0420837 (Contraception status)
    SNOMED
    243816001
    women able to have children must have a negative pregnancy test 14 days before study enrollment
    Descripción

    negative pregnancy test

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0427780 (Pregnancy test negative)
    SNOMED
    250425007
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    patients with prior treatment with other investigational agents less than 4 weeks before study enrollment
    Descripción

    investigational agents

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1875319 (INVESTIGATIONAL AGENTS)
    pregnant or nursing female patients
    Descripción

    pregnancy; lactating

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    UMLS CUI [1,2]
    C0006147 (Breast Feeding)
    SNOMED
    169741004
    LOINC
    LP420040-0
    patients who are hiv positive
    Descripción

    hiv positive

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0019699 (HIV Seropositivity)
    SNOMED
    165816005
    patients who have hepatitis a, b, or c
    Descripción

    hepatitis

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0019158 (Hepatitis)
    SNOMED
    128241005
    LOINC
    LP20771-9
    patients unable to take study medication by mouth
    Descripción

    Oral Route of Drug administration

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C1527415 (Oral Route of Drug administration)
    SNOMED
    26643006
    LOINC
    LA16023-6
    patients with untreated brain cancer
    Descripción

    brain cancer

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0153633 (Malignant neoplasm of brain)
    SNOMED
    428061005
    patient eligible for treatment with bevacizumab and for whom bevacizumab is available
    Descripción

    bevacizumab

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0796392 (bevacizumab)
    SNOMED
    409405006
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    Similar models

    Eligibility Stage IIIB or IV Non-Small Cell Lung Cancer NCT00473889

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    age; non-small cell lung cancer
    Item
    males and females at least 18 years of age who have confirmed diagnosis of non-small cell lung cancer
    boolean
    C0001779 (UMLS CUI [1])
    C0007131 (UMLS CUI [2])
    therapy systemic lung cancer
    Item
    patients with no systemic prior systemic treatment for lung cancer except patients at least 12 months from prior adjuvant therapy
    boolean
    C0087111 (UMLS CUI [1,1])
    C0205373 (UMLS CUI [1,2])
    C0242379 (UMLS CUI [1,3])
    organ function adequate; liver function
    Item
    adequate bone marrow,kidney and liver function
    boolean
    C0678852 (UMLS CUI [1,1])
    C0205411 (UMLS CUI [1,2])
    C0232741 (UMLS CUI [2])
    major surgery; radiation
    Item
    must be recovered and at least 4 weeks from major surgery or radiation
    boolean
    C0679637 (UMLS CUI [1])
    C0851346 (UMLS CUI [2])
    ecog
    Item
    ecog (eastern cooperative oncology group) performance status of 0 or 1
    boolean
    C1520224 (UMLS CUI [1])
    contraception status
    Item
    men and women must agree to use birth control during the study
    boolean
    C0420837 (UMLS CUI [1])
    negative pregnancy test
    Item
    women able to have children must have a negative pregnancy test 14 days before study enrollment
    boolean
    C0427780 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    investigational agents
    Item
    patients with prior treatment with other investigational agents less than 4 weeks before study enrollment
    boolean
    C1875319 (UMLS CUI [1])
    pregnancy; lactating
    Item
    pregnant or nursing female patients
    boolean
    C0032961 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])
    hiv positive
    Item
    patients who are hiv positive
    boolean
    C0019699 (UMLS CUI [1])
    hepatitis
    Item
    patients who have hepatitis a, b, or c
    boolean
    C0019158 (UMLS CUI [1])
    Oral Route of Drug administration
    Item
    patients unable to take study medication by mouth
    boolean
    C1527415 (UMLS CUI [1])
    brain cancer
    Item
    patients with untreated brain cancer
    boolean
    C0153633 (UMLS CUI [1])
    bevacizumab
    Item
    patient eligible for treatment with bevacizumab and for whom bevacizumab is available
    boolean
    C0796392 (UMLS CUI [1])
    Volver a la parte superior de la página 

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