0 Bedömningar
ID

28277

Beskrivning

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. Visit: All visits. Source: Prof. Dr. med. Georg Heß Universitätsmedizin Mainz

Nyckelord

Versioner (2)
  1. 2017-12-10 2017-12-10 -
  2. 2018-01-02 2018-01-02 -
Rättsinnehavare

Prof. Dr. med. Georg Heß

Uppladdad den

2 januari 2018

DOI

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Licens

Creative Commons BY-NC 3.0
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    End of study GOAL Trial B-cell Lymphoma NCT02499003

    Engelsk

    End of study GOAL Trial B-cell Lymphoma NCT02499003

    1 Formulär  
    End of study
    Beskrivning

    End of study

    Alias
    UMLS CUI-1
    C0008976
    UMLS CUI-2
    C0444930
    Subject ID
    Beskrivning

    Subject ID

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2348585
    Date of study end
    Beskrivning

    Date of study end

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C2983670
    Did the subject complete the follow-up?
    Beskrivning

    follow-up completion

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1522577
    UMLS CUI [1,2]
    C0205197
    If 'no', please specify reason(s) for early follow-up termination:
    Beskrivning

    termination reason

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C1283212
    UMLS CUI [1,2]
    C0392360
    If 'death': Date
    Beskrivning

    Date of death

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C1148348
    If 'death': Reason
    Beskrivning

    reason of death

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0007465
    If 'other' reason for early follow-up termination, please specify:
    Beskrivning

    specify

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C1521902
    Tillbaka till toppen

    Similar models

    End of study GOAL Trial B-cell Lymphoma NCT02499003

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    End of study
    C0008976 (UMLS CUI-1)
    C0444930 (UMLS CUI-2)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Date of study end
    Item
    Date of study end
    date
    C2983670 (UMLS CUI [1])
    follow-up completion
    Item
    Did the subject complete the follow-up?
    boolean
    C1522577 (UMLS CUI [1,1])
    C0205197 (UMLS CUI [1,2])
    Item
    If 'no', please specify reason(s) for early follow-up termination:
    text
    C1283212 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    early follow-up termination reason
    Code List
    If 'no', please specify reason(s) for early follow-up termination:
    CL Item
    Withdrawal of consent (Withdrawal of consent)
    C1707492 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Death (Death)
    C0011065 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Lost to Follow-Up (Lost to Follow-Up)
    C1302313 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (Other)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    Date of death
    Item
    If 'death': Date
    date
    C1148348 (UMLS CUI [1])
    Item
    If 'death': Reason
    text
    C0007465 (UMLS CUI [1])
    reason of death
    Code List
    If 'death': Reason
    CL Item
    Progression of underlying disease (Progression of underlying disease)
    C0242656 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Unknown (Unknown)
    C0439673 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (Other)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    specify
    Item
    If 'other' reason for early follow-up termination, please specify:
    text
    C1521902 (UMLS CUI [1])
    Tillbaka till toppen 

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