ID

17852

Description

Dexamethasone Compared With Prednisone During Induction Therapy and Methotrexate With or Without Leucovorin During Maintenance Therapy in Treating Patients With Newly Diagnosed High-Risk Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00075725

Link

https://clinicaltrials.gov/show/NCT00075725

Keywords

  1. 10/5/16 10/5/16 -
  2. 10/5/16 10/5/16 -
Uploaded on

October 5, 2016

DOI

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License

Creative Commons BY 4.0

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    Eligibility Leukemia NCT00075725

    Eligibility Leukemia NCT00075725

    1. StudyEvent: Eligibility
      1. Eligibility Leukemia NCT00075725
    Criteria
    Description

    Criteria

    newly diagnosed b-precursor acute lymphoblastic leukemia
    Description

    Precursor B-lymphoblastic leukaemia acute

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1737235
    wbc > 50,000/mm^3 for patients age 1 to 9
    Description

    White Blood Cell Count procedure | Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023508
    UMLS CUI [2]
    C0001779
    any wbc for patients age 10 to 30 or patients who have received prior steroid therapy or patients with testicular disease
    Description

    White Blood Cell Count procedure | Age | Steroid therapy | Testicular Disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023508
    UMLS CUI [2]
    C0001779
    UMLS CUI [3]
    C0149783
    UMLS CUI [4]
    C0039584
    must be eligible for and enrolled on classification study cog-aall03b1
    Description

    ALL Clinical Trial classification eligible | ALL Clinical Trial classification Enrollment

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0023449
    UMLS CUI [1,2]
    C0008976
    UMLS CUI [1,3]
    C0683326
    UMLS CUI [1,4]
    C1548635
    UMLS CUI [2,1]
    C0023449
    UMLS CUI [2,2]
    C0008976
    UMLS CUI [2,3]
    C0683326
    UMLS CUI [2,4]
    C1516879
    patient characteristics:
    Description

    Client Characteristics

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0815172
    1 to under 31
    Description

    Age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    performance status
    Description

    performance status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1518965
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370
    life expectancy
    Description

    Life Expectancy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023671
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370
    hematopoietic
    Description

    Function Hematopoietic

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0031843
    UMLS CUI [1,2]
    C0229601
    see disease characteristics
    Description

    disease characteristic

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0599878
    hepatic
    Description

    Liver function

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0232741
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370
    renal
    Description

    Renal function

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0232804
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370
    prior concurrent therapy:
    Description

    Comorbidity

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    biologic therapy
    Description

    Biological treatment

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1531518
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370
    chemotherapy
    Description

    Chemotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    no more than 72 hours since prior intrathecal cytarabine
    Description

    Cytarabine Intrathecal

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0010711
    UMLS CUI [1,2]
    C0677897
    no other prior cytotoxic chemotherapy
    Description

    Cytotoxic Chemotherapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0677881
    endocrine therapy
    Description

    Hormone Therapy

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0279025
    prior steroids allowed
    Description

    Steroids

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0038317
    radiotherapy
    Description

    Therapeutic radiology procedure

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370
    surgery
    Description

    Operative Surgical Procedures

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0543467
    not specified
    Description

    Unspecified

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0205370

    Similar models

    Eligibility Leukemia NCT00075725

    1. StudyEvent: Eligibility
      1. Eligibility Leukemia NCT00075725
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Precursor B-lymphoblastic leukaemia acute
    Item
    newly diagnosed b-precursor acute lymphoblastic leukemia
    boolean
    C1737235 (UMLS CUI [1])
    White Blood Cell Count procedure | Age
    Item
    wbc > 50,000/mm^3 for patients age 1 to 9
    boolean
    C0023508 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    White Blood Cell Count procedure | Age | Steroid therapy | Testicular Disease
    Item
    any wbc for patients age 10 to 30 or patients who have received prior steroid therapy or patients with testicular disease
    boolean
    C0023508 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    C0149783 (UMLS CUI [3])
    C0039584 (UMLS CUI [4])
    ALL Clinical Trial classification eligible | ALL Clinical Trial classification Enrollment
    Item
    must be eligible for and enrolled on classification study cog-aall03b1
    boolean
    C0023449 (UMLS CUI [1,1])
    C0008976 (UMLS CUI [1,2])
    C0683326 (UMLS CUI [1,3])
    C1548635 (UMLS CUI [1,4])
    C0023449 (UMLS CUI [2,1])
    C0008976 (UMLS CUI [2,2])
    C0683326 (UMLS CUI [2,3])
    C1516879 (UMLS CUI [2,4])
    Client Characteristics
    Item
    patient characteristics:
    boolean
    C0815172 (UMLS CUI [1])
    Age
    Item
    1 to under 31
    boolean
    C0001779 (UMLS CUI [1])
    performance status
    Item
    performance status
    boolean
    C1518965 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])
    Life Expectancy
    Item
    life expectancy
    boolean
    C0023671 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])
    Function Hematopoietic
    Item
    hematopoietic
    boolean
    C0031843 (UMLS CUI [1,1])
    C0229601 (UMLS CUI [1,2])
    disease characteristic
    Item
    see disease characteristics
    boolean
    C0599878 (UMLS CUI [1])
    Liver function
    Item
    hepatic
    boolean
    C0232741 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])
    Renal function
    Item
    renal
    boolean
    C0232804 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])
    Comorbidity
    Item
    prior concurrent therapy:
    boolean
    C0009488 (UMLS CUI [1])
    Biological treatment
    Item
    biologic therapy
    boolean
    C1531518 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])
    Chemotherapy
    Item
    chemotherapy
    boolean
    C0392920 (UMLS CUI [1])
    Cytarabine Intrathecal
    Item
    no more than 72 hours since prior intrathecal cytarabine
    boolean
    C0010711 (UMLS CUI [1,1])
    C0677897 (UMLS CUI [1,2])
    Cytotoxic Chemotherapy
    Item
    no other prior cytotoxic chemotherapy
    boolean
    C0677881 (UMLS CUI [1])
    Hormone Therapy
    Item
    endocrine therapy
    boolean
    C0279025 (UMLS CUI [1])
    Steroids
    Item
    prior steroids allowed
    boolean
    C0038317 (UMLS CUI [1])
    Therapeutic radiology procedure
    Item
    radiotherapy
    boolean
    C1522449 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])
    Operative Surgical Procedures
    Item
    surgery
    boolean
    C0543467 (UMLS CUI [1])
    Unspecified
    Item
    not specified
    boolean
    C0205370 (UMLS CUI [1])

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