0 Avaliações

ID

16523

Descrição

Gemcitabine/Oxaliplatin (GEMOX) vs Carboplatin/Paclitaxel (CP) in Non-Small Cell Lung Cancer (NSCLC); ODM derived from: https://clinicaltrials.gov/show/NCT00087802

Link

https://clinicaltrials.gov/show/NCT00087802

Palavras-chave

  1. 22/07/2016 22/07/2016 -
Transferido a

22 de julho de 2016

DOI

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Licença

Creative Commons BY 4.0

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    Eligibility Carcinoma, Non-Small-Cell Lung NCT00087802

    Eligibility Carcinoma, Non-Small-Cell Lung NCT00087802

    Inclusion Criteria
    Descrição

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    newly diagnosed, stage iiib or iv nsclc, chemo or other systemic therapy naive
    Descrição

    Non-Small Cell Lung Carcinoma | TNM clinical staging | Chemotherapy | Therapy naive Systemic

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0007131
    UMLS CUI [2]
    C3258246
    UMLS CUI [3]
    C0392920
    UMLS CUI [4,1]
    C0919936
    UMLS CUI [4,2]
    C0205373
    one (1) unidimensionally measurable lesion
    Descrição

    Measurable Disease Quantity | Lesion size Dimension One

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C1513041
    UMLS CUI [1,2]
    C1265611
    UMLS CUI [2,1]
    C0449453
    UMLS CUI [2,2]
    C0439534
    UMLS CUI [2,3]
    C0205447
    ecog performance status of 0 or 1, no peripheral neuropathy >grade 1
    Descrição

    ECOG performance status | Peripheral Neuropathy Grade

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    UMLS CUI [2,1]
    C0031117
    UMLS CUI [2,2]
    C0441800
    patients with clinically stable brain metastases on a stable dose of (or no longer requiring) dexamethasone at registration will be eligible. patients who have received cranial radiation for brain metastases must be at least 4 weeks from last radiation treatment.
    Descrição

    Metastatic malignant neoplasm to brain Stable Clinical | Dexamethasone Dose Stable | Cranial Irradiation Metastatic malignant neoplasm to brain

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0220650
    UMLS CUI [1,2]
    C0205360
    UMLS CUI [1,3]
    C0205210
    UMLS CUI [2,1]
    C0011777
    UMLS CUI [2,2]
    C0178602
    UMLS CUI [2,3]
    C0205360
    UMLS CUI [3,1]
    C0079172
    UMLS CUI [3,2]
    C0220650
    recovery in full from any previous surgical procedure
    Descrição

    Operative Surgical Procedures Complete Recovery

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0543467
    UMLS CUI [1,2]
    C2826210
    no history of an acute cardiac or cns event within 6 months of entry or current clinical evidence of congestive heart failure or non-stable coronary artery disease
    Descrição

    cardiac event | CNS disorder | Congestive heart failure Evidence of | Coronary Artery Disease Unstable

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0741923
    UMLS CUI [2]
    C0007682
    UMLS CUI [3,1]
    C0018802
    UMLS CUI [3,2]
    C0332120
    UMLS CUI [4,1]
    C1956346
    UMLS CUI [4,2]
    C0443343
    Exclusion Criteria
    Descrição

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    hypersensitivity to any of the 4 study drugs
    Descrição

    Hypersensitivity Investigational New Drugs

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0020517
    UMLS CUI [1,2]
    C0013230
    concurrent immunotherapy or participation in any investigational drug study within 4 weeks
    Descrição

    Immunotherapy | Study Subject Participation Status | Investigational New Drugs

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0021083
    UMLS CUI [2]
    C2348568
    UMLS CUI [3]
    C0013230
    serious uncontrolled intercurrent medical or psychiatric illness and organ allograft
    Descrição

    Comorbidity Uncontrolled Serious | Allograft Organ

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0009488
    UMLS CUI [1,2]
    C0205318
    UMLS CUI [1,3]
    C0205404
    UMLS CUI [2,1]
    C0040739
    UMLS CUI [2,2]
    C0178784
    history of other malignancy within the last 5 years (except for squamous or basal cell carcinoma of the skin, carcinoma in situ of the cervix, or superficial transitional cell carcinoma of the bladder)
    Descrição

    Malignant Neoplasms | Squamous cell carcinoma of skin | Basal cell carcinoma | Carcinoma in situ of uterine cervix | Transitional cell carcinoma of bladder Superficial

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    UMLS CUI [2]
    C0553723
    UMLS CUI [3]
    C0007117
    UMLS CUI [4]
    C0851140
    UMLS CUI [5,1]
    C0279680
    UMLS CUI [5,2]
    C0205124
    patient is a pregnant or lactating female
    Descrição

    Pregnancy | Breast Feeding

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147

    Similar models

    Eligibility Carcinoma, Non-Small-Cell Lung NCT00087802

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Non-Small Cell Lung Carcinoma | TNM clinical staging | Chemotherapy | Therapy naive Systemic
    Item
    newly diagnosed, stage iiib or iv nsclc, chemo or other systemic therapy naive
    boolean
    C0007131 (UMLS CUI [1])
    C3258246 (UMLS CUI [2])
    C0392920 (UMLS CUI [3])
    C0919936 (UMLS CUI [4,1])
    C0205373 (UMLS CUI [4,2])
    Measurable Disease Quantity | Lesion size Dimension One
    Item
    one (1) unidimensionally measurable lesion
    boolean
    C1513041 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    C0449453 (UMLS CUI [2,1])
    C0439534 (UMLS CUI [2,2])
    C0205447 (UMLS CUI [2,3])
    ECOG performance status | Peripheral Neuropathy Grade
    Item
    ecog performance status of 0 or 1, no peripheral neuropathy >grade 1
    boolean
    C1520224 (UMLS CUI [1])
    C0031117 (UMLS CUI [2,1])
    C0441800 (UMLS CUI [2,2])
    Metastatic malignant neoplasm to brain Stable Clinical | Dexamethasone Dose Stable | Cranial Irradiation Metastatic malignant neoplasm to brain
    Item
    patients with clinically stable brain metastases on a stable dose of (or no longer requiring) dexamethasone at registration will be eligible. patients who have received cranial radiation for brain metastases must be at least 4 weeks from last radiation treatment.
    boolean
    C0220650 (UMLS CUI [1,1])
    C0205360 (UMLS CUI [1,2])
    C0205210 (UMLS CUI [1,3])
    C0011777 (UMLS CUI [2,1])
    C0178602 (UMLS CUI [2,2])
    C0205360 (UMLS CUI [2,3])
    C0079172 (UMLS CUI [3,1])
    C0220650 (UMLS CUI [3,2])
    Operative Surgical Procedures Complete Recovery
    Item
    recovery in full from any previous surgical procedure
    boolean
    C0543467 (UMLS CUI [1,1])
    C2826210 (UMLS CUI [1,2])
    cardiac event | CNS disorder | Congestive heart failure Evidence of | Coronary Artery Disease Unstable
    Item
    no history of an acute cardiac or cns event within 6 months of entry or current clinical evidence of congestive heart failure or non-stable coronary artery disease
    boolean
    C0741923 (UMLS CUI [1])
    C0007682 (UMLS CUI [2])
    C0018802 (UMLS CUI [3,1])
    C0332120 (UMLS CUI [3,2])
    C1956346 (UMLS CUI [4,1])
    C0443343 (UMLS CUI [4,2])
    Item Group
    C0680251 (UMLS CUI)
    Hypersensitivity Investigational New Drugs
    Item
    hypersensitivity to any of the 4 study drugs
    boolean
    C0020517 (UMLS CUI [1,1])
    C0013230 (UMLS CUI [1,2])
    Immunotherapy | Study Subject Participation Status | Investigational New Drugs
    Item
    concurrent immunotherapy or participation in any investigational drug study within 4 weeks
    boolean
    C0021083 (UMLS CUI [1])
    C2348568 (UMLS CUI [2])
    C0013230 (UMLS CUI [3])
    Comorbidity Uncontrolled Serious | Allograft Organ
    Item
    serious uncontrolled intercurrent medical or psychiatric illness and organ allograft
    boolean
    C0009488 (UMLS CUI [1,1])
    C0205318 (UMLS CUI [1,2])
    C0205404 (UMLS CUI [1,3])
    C0040739 (UMLS CUI [2,1])
    C0178784 (UMLS CUI [2,2])
    Malignant Neoplasms | Squamous cell carcinoma of skin | Basal cell carcinoma | Carcinoma in situ of uterine cervix | Transitional cell carcinoma of bladder Superficial
    Item
    history of other malignancy within the last 5 years (except for squamous or basal cell carcinoma of the skin, carcinoma in situ of the cervix, or superficial transitional cell carcinoma of the bladder)
    boolean
    C0006826 (UMLS CUI [1])
    C0553723 (UMLS CUI [2])
    C0007117 (UMLS CUI [3])
    C0851140 (UMLS CUI [4])
    C0279680 (UMLS CUI [5,1])
    C0205124 (UMLS CUI [5,2])
    Pregnancy | Breast Feeding
    Item
    patient is a pregnant or lactating female
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])

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