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ID

9959

Beschrijving

Randomized Phase III Study of Intensive Chemotherapy with or without Dasatinib (Sprycel(TM)) in Adult Patients with Newly Diagnosed Core-Binding Factor Acute Myeloid Leukemia (CBF-AML)

Trefwoorden

  1. 04-03-15 04-03-15 -
  2. 09-03-15 09-03-15 -
  3. 23-04-15 23-04-15 -
  4. 09-12-15 09-12-15 -
  5. 11-02-16 11-02-16 -
Geüploaded op

9 maart 2015

DOI

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Licentie

Creative Commons BY-NC 3.0 Legacy

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    Concomitant Medication AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

    Concomitant Medication AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

    Concomitant Medication
    Beschrijving

    Concomitant Medication

    Point in time
    Beschrijving

    Point in time

    Datatype

    integer

    Alias
    UMLS CUI-1
    C1442880
    If Maintenance: Month
    Beschrijving

    Maintenance Month

    Datatype

    integer

    Maateenheden
    • Month
    Alias
    UMLS CUI-1
    C0481504
    UMLS CUI-2
    C0439231
    Agent/Tradename
    Beschrijving

    Agent/Tradename

    Datatype

    text

    Alias
    UMLS CUI-1
    C1254351
    UMLS CUI-2
    C0282291
    Dose
    Beschrijving

    Dose

    Datatype

    integer

    Alias
    UMLS CUI-1
    C3174092
    Unit
    Beschrijving

    Unit

    Datatype

    text

    Alias
    UMLS CUI-1
    C0869039
    Application
    Beschrijving

    Application

    Datatype

    text

    Alias
    UMLS CUI-1
    C0185125
    Frequency
    Beschrijving

    Frequency

    Datatype

    text

    Alias
    UMLS CUI-1
    C3476109
    Medical indication
    Beschrijving

    Medical indication

    Datatype

    text

    Alias
    UMLS CUI-1
    C2315323
    Start Date of Medication
    Beschrijving

    Start Date of Medication

    Datatype

    date

    Alias
    UMLS CUI-1
    C0808070
    UMLS CUI-2
    C0802004
    Stop Date Medication
    Beschrijving

    Stop Date

    Datatype

    date

    Alias
    UMLS CUI-1
    C0802004
    UMLS CUI-2
    C0806020
    Signature
    Beschrijving

    Signature

    Date
    Beschrijving

    Date

    Datatype

    date

    Alias
    UMLS CUI-1
    C0011008
    Name of Investigator
    Beschrijving

    Name of Investigator

    Datatype

    text

    Alias
    UMLS CUI-1
    C2826892
    Signature of investigator
    Beschrijving

    Signature of investigator

    Datatype

    text

    Alias
    UMLS CUI-1
    C2346576

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    Concomitant Medication AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Concomitant Medication
    Item
    Point in time
    integer
    C1442880 (UMLS CUI-1)
    Code List
    Point in time
    CL Item
    Diagnostic (0)
    CL Item
    Induction I (1)
    CL Item
    Induction II (optional) (2)
    CL Item
    Consolid. I (3)
    CL Item
    Consolid. II (4)
    CL Item
    Consolid. III (5)
    CL Item
    Consolid. IV (6)
    CL Item
    Maintenance (7)
    Item
    If Maintenance: Month
    integer
    C0481504 (UMLS CUI-1)
    C0439231 (UMLS CUI-2)
    Code List
    If Maintenance: Month
    CL Item
    after 1 Month (1)
    CL Item
    after 2 Month (2)
    CL Item
    after 3 Month (3)
    CL Item
    after 4 Month (4)
    CL Item
    after 5 Month (5)
    CL Item
    after 6 Month (6)
    CL Item
    after 7 Month (7)
    CL Item
    after 8 Month (8)
    CL Item
    after 9 Month (9)
    CL Item
    after 10 Month (10)
    CL Item
    after 11 Month (11)
    CL Item
    after 12 Month (12)
    Agent/Tradename
    Item
    Agent/Tradename
    text
    C1254351 (UMLS CUI-1)
    C0282291 (UMLS CUI-2)
    Dose
    Item
    Dose
    integer
    C3174092 (UMLS CUI-1)
    Unit
    Item
    Unit
    text
    C0869039 (UMLS CUI-1)
    Item
    Application
    text
    C0185125 (UMLS CUI-1)
    Code List
    Application
    CL Item
    oral (1)
    CL Item
    intravenous (2)
    CL Item
    intramuscular (3)
    CL Item
    subcutaneous (4)
    CL Item
    sublingual (5)
    CL Item
    rectal (6)
    CL Item
    Inhalation (7)
    CL Item
    topical (8)
    CL Item
    other (9)
    Frequency
    Item
    Frequency
    text
    C3476109 (UMLS CUI-1)
    Medical indication
    Item
    Medical indication
    text
    C2315323 (UMLS CUI-1)
    Start Date of Medication
    Item
    Start Date of Medication
    date
    C0808070 (UMLS CUI-1)
    C0802004 (UMLS CUI-2)
    Stop Date
    Item
    Stop Date Medication
    date
    C0802004 (UMLS CUI-1)
    C0806020 (UMLS CUI-2)
    Item Group
    Signature
    Date
    Item
    Date
    date
    C0011008 (UMLS CUI-1)
    Name of Investigator
    Item
    Name of Investigator
    text
    C2826892 (UMLS CUI-1)
    Signature of investigator
    Item
    Signature of investigator
    text
    C2346576 (UMLS CUI-1)

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