0 Ratings

ID

28277

Description

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

Keywords

  1. 12/10/17 12/10/17 -
  2. 1/2/18 1/2/18 -
Copyright Holder

Prof. Dr. med. Georg Heß

Uploaded on

January 2, 2018

DOI

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License

Creative Commons BY-NC 3.0

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    End of study GOAL Trial B-cell Lymphoma NCT02499003

    End of study GOAL Trial B-cell Lymphoma NCT02499003

    End of study
    Description

    End of study

    Alias
    UMLS CUI-1
    C0008976 (Clinical Trials)
    SNOMED
    110465008
    LOINC
    LP231796-6
    UMLS CUI-2
    C0444930 (End)
    SNOMED
    261782000
    Subject ID
    Description

    Subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Date of study end
    Description

    Date of study end

    Data type

    date

    Alias
    UMLS CUI [1]
    C2983670 (Study End Date)
    Did the subject complete the follow-up?
    Description

    follow-up completion

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1522577 (follow-up)
    UMLS CUI [1,2]
    C0205197 (Complete)
    SNOMED
    255594003
    LOINC
    LA13937-0
    If 'no', please specify reason(s) for early follow-up termination:
    Description

    termination reason

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C1283212 (Termination - action)
    SNOMED
    360239007
    UMLS CUI [1,2]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    If 'death': Date
    Description

    Date of death

    Data type

    date

    Alias
    UMLS CUI [1]
    C1148348 (Date of death)
    SNOMED
    399753006
    LOINC
    MTHU014693
    If 'death': Reason
    Description

    reason of death

    Data type

    text

    Alias
    UMLS CUI [1]
    C0007465 (Cause of Death)
    SNOMED
    16100001
    LOINC
    LA10595-9
    If 'other' reason for early follow-up termination, please specify:
    Description

    specify

    Data type

    text

    Alias
    UMLS CUI [1]
    C1521902 (To specify)

    Similar models

    End of study GOAL Trial B-cell Lymphoma NCT02499003

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    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])
    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])
    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])

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