0 Evaluaciones

ID

13978

Descripción

Study part: Study end.Observational study on CML patients in any phase treated with ponatinib (Iclusig®) at any dose. Principal Investigator Prof. Dr. A. Hochhaus.

Palabras clave

  1. 20/3/16 20/3/16 -
Subido en

20 de marzo de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0

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    Study end Ponderosa CML ZKSJ0083

    1. StudyEvent: ODM
      1. Study end
    Patient status
    Descripción

    Patient status

    Alias
    UMLS CUI-1
    C0449437 (Patient status)
    SNOMED
    246097001
    Date of contact with patients
    Descripción

    date

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0011008 (Date in time)
    SNOMED
    410671006
    UMLS CUI [1,2]
    C0332158 (Contact with)
    SNOMED
    11723008
    Patient status
    Descripción

    Patient status

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0449437 (Patient status)
    SNOMED
    246097001
    If other status, please mention:
    Descripción

    Other

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0205394 (Other)
    SNOMED
    74964007
    LOINC
    LP21049-9
    Date of death
    Descripción

    death date

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C1148348 (Date of death)
    SNOMED
    399753006
    LOINC
    MTHU014693
    Cause of death
    Descripción

    cause of death

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0007465 (Cause of Death)
    SNOMED
    16100001
    LOINC
    LA10595-9

    Similar models

    Study end

    1. StudyEvent: ODM
      1. Study end
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Patient status
    C0449437 (UMLS CUI-1)
    date
    Item
    Date of contact with patients
    date
    C0011008 (UMLS CUI [1,1])
    C0332158 (UMLS CUI [1,2])
    Item
    Patient status
    text
    C0449437 (UMLS CUI [1])
    Code List
    Patient status
    CL Item
    Patient lives on the day of the Follow-Up (1)
    CL Item
    Patient status at the time of follow-up unknown (Establishment of contact is further attempted) (2)
    CL Item
    Lost to follow-up  (3)
    CL Item
    Informed consent withdrawn (4)
    CL Item
    Dead (5)
    CL Item
    Completed study period (6)
    CL Item
    Discontinuation of Sponsor (7)
    CL Item
    Other status (8)
    Other
    Item
    If other status, please mention:
    text
    C0205394 (UMLS CUI [1])
    death date
    Item
    Date of death
    date
    C1148348 (UMLS CUI [1])
    cause of death
    Item
    Cause of death
    text
    C0007465 (UMLS CUI [1])

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