0 Ratings

ID

12921

Description

Gene Therapy Plus Chemotherapy in Treating Patients With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00004038

Link

https://clinicaltrials.gov/show/NCT00004038

Keywords

  1. 1/6/16 1/6/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 6, 2016

DOI

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License

Creative Commons BY-NC 3.0

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    Eligibility Breast Cancer NCT00004038

    Eligibility Breast Cancer NCT00004038

    Criteria
    Description

    Criteria

    histologically confirmed epithelial breast cancer
    Description

    breast cancer

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0678222
    at least 3 cutaneous or subcutaneous lesions required
    Description

    cutaneous or subcutaneous lesions

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0221198
    measurable disease that includes, but is not limited to, cutaneous or subcutaneous metastases
    Description

    measurable disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1513041
    patient characteristics:
    Description

    patient characteristics

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0815172
    age: over 18
    Description

    age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    performance status: ecog 0-2
    Description

    performance status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    absolute granulocyte count at least 1,500/mm3
    Description

    absolute granulocyte count

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0857490
    hemoglobin greater than 8 g/dl
    Description

    hemoglobin

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0019046
    platelet count greater than 100,000/mm3
    Description

    platelet count

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0005821
    bilirubin less than 2 mg/dl
    Description

    bilirubin

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1278039
    pt/ptt within normal range
    Description

    pt/ptt

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0030605
    sgot/sgpt less than 2 times upper limit of normal
    Description

    sgot/sgpt

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0201836
    UMLS CUI [2]
    C0201899
    creatinine less than 1.8 mg/dl
    Description

    creatinine

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0201976
    not pregnant
    Description

    pregnant

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    fertile patients must use effective contraception during and for 3 months after therapy
    Description

    contraception

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0700589
    prior concurrent therapy:
    Description

    prior concurrent therapy:

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0087111
    concurrent cytotoxic chemotherapy allowed, if stable and responding
    Description

    chemotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    at least 4 weeks since prior chemotherapy, if starting a new regimen
    Description

    at least 4 weeks since prior chemotherapy, if starting a new regimen

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    at least 4 weeks since radiotherapy
    Description

    radiotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    prior adjuvant radiotherapy to the chest wall allowed
    Description

    prior adjuvant radiotherapy to the chest wall allowed

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    at least 6 months since radiotherapy to lesions that are to be injected
    Description

    at least 6 months since radiotherapy to lesions that are to be injected

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    recovered from prior therapy
    Description

    recovered from prior therapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0087111

    Similar models

    Eligibility Breast Cancer NCT00004038

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    breast cancer
    Item
    histologically confirmed epithelial breast cancer
    boolean
    C0678222 (UMLS CUI [1])
    cutaneous or subcutaneous lesions
    Item
    at least 3 cutaneous or subcutaneous lesions required
    boolean
    C0221198 (UMLS CUI [1])
    measurable disease
    Item
    measurable disease that includes, but is not limited to, cutaneous or subcutaneous metastases
    boolean
    C1513041 (UMLS CUI [1])
    patient characteristics
    Item
    patient characteristics:
    boolean
    C0815172 (UMLS CUI [1])
    age
    Item
    age: over 18
    boolean
    C0001779 (UMLS CUI [1])
    performance status
    Item
    performance status: ecog 0-2
    boolean
    C1520224 (UMLS CUI [1])
    absolute granulocyte count
    Item
    absolute granulocyte count at least 1,500/mm3
    boolean
    C0857490 (UMLS CUI [1])
    hemoglobin
    Item
    hemoglobin greater than 8 g/dl
    boolean
    C0019046 (UMLS CUI [1])
    platelet count
    Item
    platelet count greater than 100,000/mm3
    boolean
    C0005821 (UMLS CUI [1])
    bilirubin
    Item
    bilirubin less than 2 mg/dl
    boolean
    C1278039 (UMLS CUI [1])
    pt/ptt
    Item
    pt/ptt within normal range
    boolean
    C0030605 (UMLS CUI [1])
    sgot/sgpt
    Item
    sgot/sgpt less than 2 times upper limit of normal
    boolean
    C0201836 (UMLS CUI [1])
    C0201899 (UMLS CUI [2])
    creatinine
    Item
    creatinine less than 1.8 mg/dl
    boolean
    C0201976 (UMLS CUI [1])
    pregnant
    Item
    not pregnant
    boolean
    C0032961 (UMLS CUI [1])
    contraception
    Item
    fertile patients must use effective contraception during and for 3 months after therapy
    boolean
    C0700589 (UMLS CUI [1])
    prior concurrent therapy:
    Item
    prior concurrent therapy:
    boolean
    C0087111 (UMLS CUI [1])
    chemotherapy
    Item
    concurrent cytotoxic chemotherapy allowed, if stable and responding
    boolean
    C0392920 (UMLS CUI [1])
    at least 4 weeks since prior chemotherapy, if starting a new regimen
    Item
    at least 4 weeks since prior chemotherapy, if starting a new regimen
    boolean
    C0392920 (UMLS CUI [1])
    radiotherapy
    Item
    at least 4 weeks since radiotherapy
    boolean
    C1522449 (UMLS CUI [1])
    prior adjuvant radiotherapy to the chest wall allowed
    Item
    prior adjuvant radiotherapy to the chest wall allowed
    boolean
    C1522449 (UMLS CUI [1])
    at least 6 months since radiotherapy to lesions that are to be injected
    Item
    at least 6 months since radiotherapy to lesions that are to be injected
    boolean
    C1522449 (UMLS CUI [1])
    recovered from prior therapy
    Item
    recovered from prior therapy
    boolean
    C0087111 (UMLS CUI [1])

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