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ID

17931

Description

Iressa in Poor Performance Status Patients With Previously Untreated Advanced Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193336

Lien

https://clinicaltrials.gov/show/NCT00193336

Mots-clés

Versions (1)
  1. 10/10/2016 10/10/2016 -
Téléchargé le

10 octobre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility Lung Cancer NCT00193336

    Anglais

    Eligibility Lung Cancer NCT00193336

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

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

    criteria Fulfill

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0243161
    UMLS CUI [1,2]
    C1550543
    biopsy proven non-small cell lung cancer
    Description

    Non-Small Cell Lung Carcinoma | Biopsy

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0007131
    UMLS CUI [2]
    C0005558
    recurrent non-small cell lung cancer after previous surgery or radiation
    Description

    Non-small cell lung cancer recurrent | Operative Surgical Procedures | Therapeutic radiology procedure

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0278517
    UMLS CUI [2]
    C0543467
    UMLS CUI [3]
    C1522449
    advanced disease (stage iiib or iv)
    Description

    advanced disease | TNM clinical staging

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0679246
    UMLS CUI [2]
    C3258246
    no previous chemotherapy or biological therapy
    Description

    Prior Chemotherapy | Biological treatment

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1514457
    UMLS CUI [2]
    C1531518
    require significant assistance with activities of daily living
    Description

    Assisting with activity of daily living Significant Patient need for

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0509063
    UMLS CUI [1,2]
    C0750502
    UMLS CUI [1,3]
    C0686904
    measurable disease
    Description

    Measurable Disease

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1513041
    adequate bone marrow, liver and kidney function
    Description

    Bone Marrow function | Liver function | Normal renal function

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0005953
    UMLS CUI [1,2]
    C0031843
    UMLS CUI [2]
    C0232741
    UMLS CUI [3]
    C0232805
    give written informed consent
    Description

    Informed Consent

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Description

    Exclusion Criteria

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

    Study Subject Participation Status

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    brain metastasis
    Description

    Metastatic malignant neoplasm to brain

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0220650
    meningeal metastasis
    Description

    Metastatic Malignant Neoplasm to the Leptomeninges

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1704231
    other uncontrolled malignancies
    Description

    Malignant Neoplasms Uncontrolled

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0006826
    UMLS CUI [1,2]
    C0205318
    women pregnant or lactating
    Description

    Pregnancy | Breast Feeding

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    no measurable disease outside previous radiation therapy field
    Description

    Involved-Field Radiation Therapy | Measurable Disease Extra-location

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C3826993
    UMLS CUI [2,1]
    C1513041
    UMLS CUI [2,2]
    C0442083
    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.
    Description

    criteria Study Protocol | Study Subject Participation Status

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0243161
    UMLS CUI [1,2]
    C2348563
    UMLS CUI [2]
    C2348568
    Retour au début de la page

    Similar models

    Eligibility Lung Cancer NCT00193336

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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])
    Non-Small Cell Lung Carcinoma | Biopsy
    Item
    biopsy proven non-small cell lung cancer
    boolean
    C0007131 (UMLS CUI [1])
    C0005558 (UMLS CUI [2])
    Non-small cell lung cancer recurrent | Operative Surgical Procedures | Therapeutic radiology procedure
    Item
    recurrent non-small cell lung cancer after previous surgery or radiation
    boolean
    C0278517 (UMLS CUI [1])
    C0543467 (UMLS CUI [2])
    C1522449 (UMLS CUI [3])
    advanced disease | TNM clinical staging
    Item
    advanced disease (stage iiib or iv)
    boolean
    C0679246 (UMLS CUI [1])
    C3258246 (UMLS CUI [2])
    Prior Chemotherapy | Biological treatment
    Item
    no previous chemotherapy or biological therapy
    boolean
    C1514457 (UMLS CUI [1])
    C1531518 (UMLS CUI [2])
    Assisting with activity of daily living Significant Patient need for
    Item
    require significant assistance with activities of daily living
    boolean
    C0509063 (UMLS CUI [1,1])
    C0750502 (UMLS CUI [1,2])
    C0686904 (UMLS CUI [1,3])
    Measurable Disease
    Item
    measurable disease
    boolean
    C1513041 (UMLS CUI [1])
    Bone Marrow function | Liver function | Normal 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])
    C0232805 (UMLS CUI [3])
    Informed Consent
    Item
    give written informed consent
    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])
    Metastatic malignant neoplasm to brain
    Item
    brain metastasis
    boolean
    C0220650 (UMLS CUI [1])
    Metastatic Malignant Neoplasm to the Leptomeninges
    Item
    meningeal metastasis
    boolean
    C1704231 (UMLS CUI [1])
    Malignant Neoplasms Uncontrolled
    Item
    other uncontrolled malignancies
    boolean
    C0006826 (UMLS CUI [1,1])
    C0205318 (UMLS CUI [1,2])
    Pregnancy | Breast Feeding
    Item
    women pregnant or lactating
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Involved-Field Radiation Therapy | Measurable Disease Extra-location
    Item
    no measurable disease outside previous radiation therapy field
    boolean
    C3826993 (UMLS CUI [1])
    C1513041 (UMLS CUI [2,1])
    C0442083 (UMLS CUI [2,2])
    criteria Study Protocol | 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
    C0243161 (UMLS CUI [1,1])
    C2348563 (UMLS CUI [1,2])
    C2348568 (UMLS CUI [2])
    Retour au début de la page 

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