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ID

28336

Beschrijving

NCT02499003 The GOAL Trial: Rescue Treatment With the Monoclonal Anti CD20-antibody Obinutuzumab (GA101) in Combination With Pixantrone for the Treatment of Patients With Relapsed Aggressive B-cell Lymphoma Source: Prof. Dr. med. Georg Heß Universitätsmedizin Mainz

Trefwoorden

Versies (2)
  1. 30-11-17 30-11-17 -
  2. 04-01-18 04-01-18 -
Houder van rechten

Prof. Dr. med. Georg Heß

Geüploaded op

4 januari 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Screening Registration GOAL Trial B-cell Lymphoma NCT02499003

    Engels

    Screening Registration GOAL Trial B-cell Lymphoma NCT02499003

    1 Formulieren  
    Admininstrative data
    Beschrijving

    Admininstrative data

    Alias
    UMLS CUI-1
    C1320722
    Subject ID
    Beschrijving

    Subject ID

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2348585
    Registration
    Beschrijving

    Registration

    Alias
    UMLS CUI-1
    C1514821
    Subject complies with all inclusion criteria?
    Beschrijving

    compliance inclusion criteria

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C1512693
    Subject complies with all exclusion criteria?
    Beschrijving

    compliance exclusion criteria

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0680251
    Include subject into study?
    Beschrijving

    In case of non-inclusion, please fill out the End of Study form

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1512693
    UMLS CUI [1,2]
    C2348563
    Patient No.
    Beschrijving

    Patient number

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C1830427
    Terug naar het begin van de pagina

    Similar models

    Screening Registration GOAL Trial B-cell Lymphoma NCT02499003

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Admininstrative data
    C1320722 (UMLS CUI-1)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Item Group
    Registration
    C1514821 (UMLS CUI-1)
    compliance inclusion criteria
    Item
    Subject complies with all inclusion criteria?
    boolean
    C1321605 (UMLS CUI [1,1])
    C1512693 (UMLS CUI [1,2])
    compliance exclusion criteria
    Item
    Subject complies with all exclusion criteria?
    boolean
    C1321605 (UMLS CUI [1,1])
    C0680251 (UMLS CUI [1,2])
    Inclusion in study
    Item
    Include subject into study?
    boolean
    C1512693 (UMLS CUI [1,1])
    C2348563 (UMLS CUI [1,2])
    Patient number
    Item
    Patient No.
    integer
    C1830427 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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