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ID

12674

Description

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)

Keywords

Versions (5)
  1. 3/4/15 3/4/15 -
  2. 3/9/15 3/9/15 -
  3. 4/23/15 4/23/15 -
  4. 12/9/15 12/9/15 -
  5. 2/11/16 2/11/16 -
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December 9, 2015

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Creative Commons BY-NC 3.0
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    Concomitant Medication AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

    English

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

    1 forms  
    Concomitant Medication
    Description

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852 (Concomitant Agent)
    Point in time
    Description

    Point in time

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C1276413 (Therapeutic regimen)
    SNOMED
    133877004
    UMLS CUI [1,2]
    C2348792 (Timepoint)
    If Maintenance: Month
    Description

    Maintenance Month

    Data type

    integer

    Measurement units
    • Month
    Alias
    UMLS CUI [1,1]
    C0481504 (Maintenance Chemotherapy)
    UMLS CUI [1,2]
    C0439231 (month)
    SNOMED
    258706009
    Pharmalogical Substance
    Description

    Pharmalogical Substance

    Data type

    text

    Alias
    UMLS CUI [1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    Dose
    Description

    Dose

    Data type

    integer

    Alias
    UMLS CUI [1]
    C3174092 (Medication dose)
    LOINC
    LP116765-1
    Unit
    Description

    Unit

    Data type

    text

    Alias
    UMLS CUI-1
    C0869039 (Unit dose)
    SNOMED
    408102007
    Application
    Description

    Application

    Data type

    text

    Alias
    UMLS CUI [1]
    C0185125 (Application procedure)
    SNOMED
    410618006
    Frequency
    Description

    Frequency

    Data type

    text

    Alias
    UMLS CUI [1]
    C3476109 (Medication frequency)
    LOINC
    LP149758-7
    Medical indication
    Description

    Medical indication

    Data type

    text

    Alias
    UMLS CUI-1
    C2315323 (Indication for procedure)
    SNOMED
    432678004
    Start Date of Medication
    Description

    Start Date of Medication

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0808070 (Start Date)
    Stop Date Medication
    Description

    Stop Date

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0013227 (Pharmaceutical Preparations)
    SNOMED
    763158003
    LOINC
    LP100609-9
    UMLS CUI [1,2]
    C0806020 (End date)
    SNOMED
    454551000124105
    LOINC
    MTHU008302
    Signature
    Description

    Signature

    Date
    Description

    Date

    Data type

    date

    Alias
    UMLS CUI-1
    C0011008 (Date in time)
    SNOMED
    410671006
    Name of Investigator
    Description

    Name of Investigator

    Data type

    text

    Alias
    UMLS CUI-1
    C2826892 (Investigator Name)
    Signature of investigator
    Description

    Signature of investigator

    Data type

    text

    Alias
    UMLS CUI-1
    C2346576 (Investigator Signature)
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    Similar models

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

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    Item
    Point in time
    integer
    C1276413 (UMLS CUI [1,1])
    C2348792 (UMLS CUI [1,2])
    Point in time
    Code List
    Point in time
    CL Item
    Diagnostic (0)
    C0086143 (UMLS CUI-1)
    CL Item
    Induction I (1)
    C3179010 (UMLS CUI-1)
    CL Item
    Induction II (optional) (2)
    C3179010 (UMLS CUI-1)
    CL Item
    Consolid. I (3)
    C3179017 (UMLS CUI-1)
    CL Item
    Consolid. II (4)
    C3179017 (UMLS CUI-1)
    CL Item
    Consolid. III (5)
    C3179017 (UMLS CUI-1)
    CL Item
    Consolid. IV (6)
    C3179017 (UMLS CUI-1)
    CL Item
    Maintenance (7)
    C0481504 (UMLS CUI-1)
    Item
    If Maintenance: Month
    integer
    C0481504 (UMLS CUI [1,1])
    C0439231 (UMLS CUI [1,2])
    Maintenance Month
    Code List
    If Maintenance: Month
    CL Item
    after 1 Month (1)
    C0439231 (UMLS CUI-1)
    C0205447 (UMLS CUI-2)
    CL Item
    after 2 Month (2)
    C0439231 (UMLS CUI-1)
    C0205448 (UMLS CUI-2)
    CL Item
    after 3 Month (3)
    C0439231 (UMLS CUI-1)
    C0205449 (UMLS CUI-2)
    CL Item
    after 4 Month (4)
    C0439231 (UMLS CUI-1)
    C0205450 (UMLS CUI-2)
    CL Item
    after 5 Month (5)
    C0439231 (UMLS CUI-1)
    C0205451 (UMLS CUI-2)
    CL Item
    after 6 Month (6)
    C0439231 (UMLS CUI-1)
    C0205452 (UMLS CUI-2)
    CL Item
    after 7 Month (7)
    C0439231 (UMLS CUI-1)
    C0205453 (UMLS CUI-2)
    CL Item
    after 8 Month (8)
    C0439231 (UMLS CUI-1)
    C0205454 (UMLS CUI-2)
    CL Item
    after 9 Month (9)
    C0439231 (UMLS CUI-1)
    C0205455 (UMLS CUI-2)
    CL Item
    after 10 Month (10)
    C0439231 (UMLS CUI-1)
    C0205456 (UMLS CUI-2)
    CL Item
    after 11 Month (11)
    C0439231 (UMLS CUI-1)
    C0205457 (UMLS CUI-2)
    CL Item
    after 12 Month (12)
    C0439231 (UMLS CUI-1)
    C0205458 (UMLS CUI-2)
    Pharmalogical Substance
    Item
    Pharmalogical Substance
    text
    C0013227 (UMLS CUI [1])
    Dose
    Item
    Dose
    integer
    C3174092 (UMLS CUI [1])
    Unit
    Item
    Unit
    text
    C0869039 (UMLS CUI-1)
    Item
    Application
    text
    C0185125 (UMLS CUI [1])
    Application
    Code List
    Application
    CL Item
    oral (1)
    C0442027 (UMLS CUI-1)
    CL Item
    intravenous (2)
    C0348016 (UMLS CUI-1)
    CL Item
    intramuscular (3)
    C0442117 (UMLS CUI-1)
    CL Item
    subcutaneous (4)
    C0443315 (UMLS CUI-1)
    CL Item
    sublingual (5)
    C0001565 (UMLS CUI-1)
    CL Item
    rectal (6)
    C0205052 (UMLS CUI-1)
    CL Item
    Inhalation (7)
    C0205535 (UMLS CUI-1)
    CL Item
    topical (8)
    C0332237 (UMLS CUI-1)
    CL Item
    other (9)
    C0205394 (UMLS CUI-1)
    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
    C0013227 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    Stop Date
    Item
    Stop Date Medication
    date
    C0013227 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    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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