0 Evaluaciones
ID

13475

Descripción

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)

Palabras clave

Versiones (5)
  1. 5/3/15 5/3/15 -
  2. 9/3/15 9/3/15 -
  3. 24/4/15 24/4/15 -
  4. 15/12/15 15/12/15 -
  5. 11/2/16 11/2/16 -
Subido en

11 de febrero de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0
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    End of Study AMLSG 21-13 DRKS00007189 NCT02013648 Akute myeloische Leukämie (AML)

    Inglés

    End of Study AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

    1 formularios  
    End of Study
    Descripción

    End of Study

    End of Study Date
    Descripción

    End of Study Date

    Tipo de datos

    date

    Alias
    UMLS CUI-1
    C2983670
    Reason for End of Study
    Descripción

    Reason for End of Study

    Tipo de datos

    integer

    Alias
    UMLS CUI-1
    C2348577
    Specify if Reason for End of Study = 6 or 7
    Descripción

    Specify if Reason for End of Study = 6 or 7

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C1521902
    Induction therapy I administered
    Descripción

    Induction therapy I administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3179010
    UMLS CUI [1,2]
    C0806914
    UMLS CUI [1,3]
    C0205447
    Induction therapy II administered
    Descripción

    Induction therapy II administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3179010
    UMLS CUI [1,2]
    C0806914
    UMLS CUI [1,3]
    C0205448
    Consolidation therapy I administered
    Descripción

    Consolidation therapy I administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3179017
    UMLS CUI [1,2]
    C0806914
    UMLS CUI [1,3]
    C0205447
    Consolidation therapy II administered
    Descripción

    Consolidation therapy II administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3179017
    UMLS CUI [1,2]
    C0806914
    UMLS CUI [1,3]
    C0205448
    Consolidation therapy III administered
    Descripción

    Consolidation therapy III administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3179017
    UMLS CUI [1,2]
    C0806914
    UMLS CUI [1,3]
    C0205449
    Consolidation therapy IV administered
    Descripción

    Consolidation therapy IV administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3179017
    UMLS CUI [1,2]
    C0806914
    UMLS CUI [1,3]
    C0205450
    Maintenance therapy administered
    Descripción

    Maintenance therapy administered

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0481504
    UMLS CUI [1,2]
    C0806914
    Signature
    Descripción

    Signature

    Date
    Descripción

    Date

    Tipo de datos

    date

    Alias
    UMLS CUI-1
    C0011008
    Name of Investigator
    Descripción

    Name of Investigator

    Tipo de datos

    text

    Alias
    UMLS CUI-1
    C2826892
    Signature of investigator
    Descripción

    Signature of investigator

    Tipo de datos

    text

    Alias
    UMLS CUI-1
    C2346576
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    Similar models

    End of Study AMLSG 21-13 NCT02013648 Akute myeloische Leukämie (AML)

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    End of Study
    End of Study Date
    Item
    End of Study Date
    date
    C2983670 (UMLS CUI-1)
    Item
    Reason for End of Study
    integer
    C2348577 (UMLS CUI-1)
    Reason for End of Study
    Code List
    Reason for End of Study
    CL Item
    regular End of Study (0)
    C0205272 (UMLS CUI-1)
    CL Item
    no CR after Induction (Progressive Disease) (1)
    C1335499 (UMLS CUI-1)
    CL Item
    exzessive extramedullary medical toxicity (2)
    C0013221 (UMLS CUI-1)
    CL Item
    death (3)
    C0021430 (UMLS CUI-1)
    CL Item
    relapse after CR (4)
    C0035020 (UMLS CUI-1)
    CL Item
    Withdrawal of informed consent (5)
    C0021430 (UMLS CUI-1)
    C1710677 (UMLS CUI-2)
    CL Item
    Protocol deviation (6)
    C1705236 (UMLS CUI-1)
    CL Item
    other (7)
    C0205394 (UMLS CUI-1)
    Specify if Reason for End of Study = 6 or 7
    Item
    Specify if Reason for End of Study = 6 or 7
    text
    C1521902 (UMLS CUI [1])
    Induction therapy I administered
    Item
    Induction therapy I administered
    boolean
    C3179010 (UMLS CUI [1,1])
    C0806914 (UMLS CUI [1,2])
    C0205447 (UMLS CUI [1,3])
    Induction therapy II administered
    Item
    Induction therapy II administered
    boolean
    C3179010 (UMLS CUI [1,1])
    C0806914 (UMLS CUI [1,2])
    C0205448 (UMLS CUI [1,3])
    Consolidation therapy I administered
    Item
    Consolidation therapy I administered
    boolean
    C3179017 (UMLS CUI [1,1])
    C0806914 (UMLS CUI [1,2])
    C0205447 (UMLS CUI [1,3])
    Consolidation therapy II administered
    Item
    Consolidation therapy II administered
    boolean
    C3179017 (UMLS CUI [1,1])
    C0806914 (UMLS CUI [1,2])
    C0205448 (UMLS CUI [1,3])
    Consolidation therapy III administered
    Item
    Consolidation therapy III administered
    boolean
    C3179017 (UMLS CUI [1,1])
    C0806914 (UMLS CUI [1,2])
    C0205449 (UMLS CUI [1,3])
    Consolidation therapy IV administered
    Item
    Consolidation therapy IV administered
    boolean
    C3179017 (UMLS CUI [1,1])
    C0806914 (UMLS CUI [1,2])
    C0205450 (UMLS CUI [1,3])
    Maintenance therapy administered
    Item
    Maintenance therapy administered
    boolean
    C0481504 (UMLS CUI [1,1])
    C0806914 (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)
    Volver a la parte superior de la página 

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