0 Ratings
ID

28253

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 Source: Prof. Dr. med. Georg Heß Universitätsmedizin Mainz

Keywords

Versions (3)
  1. 11/30/17 11/30/17 -
  2. 12/4/17 12/4/17 -
  3. 12/31/17 12/31/17 -
Copyright Holder

Prof. Dr. med. Georg Heß

Uploaded on

December 31, 2017

DOI

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License

Creative Commons BY-NC 3.0
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    Vital signs GOAL Trial B-cell Lymphoma NCT02499003

    English

    Vital signs GOAL Trial B-cell Lymphoma NCT02499003

    1 forms  
    Administrative data
    Description

    Administrative data

    Alias
    UMLS CUI-1
    C1320722
    Subject ID
    Description

    Subject ID

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348585
    Visit
    Description

    Visit

    Data type

    text

    Alias
    UMLS CUI [1]
    C0545082
    Vital signs
    Description

    Vital signs

    Alias
    UMLS CUI-1
    C0518766
    Date
    Description

    Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C0011008
    Blood Pressure Systolic
    Description

    Blood Pressure Systolic

    Data type

    integer

    Alias
    UMLS CUI [1]
    C0871470
    Blood Pressure Diastolic
    Description

    Blood Pressure Diastolic

    Data type

    integer

    Alias
    UMLS CUI [1]
    C0428883
    Pulse
    Description

    Pulse

    Data type

    integer

    Alias
    UMLS CUI [1]
    C0232117
    Body Temperature
    Description

    Body Temperature

    Data type

    float

    Measurement units
    • °C
    Alias
    UMLS CUI [1]
    C0005903
    °C
    ECOG
    Description

    Item only applies to the following visits: Screening, Day 1 of Cycles 2 - 6, Interim Staging, End of Treatment, and Follow Up 1 - 8.

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1520224
    Weight
    Description

    Item only applies to the following visits: Screening, Day 1 of Cycles 2 - 6, Interim Staging, End of Treatment, and Follow Up 1 - 8.

    Data type

    float

    Measurement units
    • kg
    Alias
    UMLS CUI [1]
    C0005910
    kg
    Height
    Description

    Item only applies to Screening.

    Data type

    float

    Measurement units
    • cm
    Alias
    UMLS CUI [1]
    C0005890
    cm
    Cycle day not done
    Description

    Item only applies to visits during Cycles 1 - 6 (Day 1, 8, 15, or 22; except Cycle 1 Day 1).

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0237753
    UMLS CUI [1,2]
    C0439228
    UMLS CUI [1,3]
    C0750729
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    Similar models

    Vital signs GOAL Trial B-cell Lymphoma NCT02499003

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative data
    C1320722 (UMLS CUI-1)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Item
    Visit
    text
    C0545082 (UMLS CUI [1])
    Visit
    Code List
    Visit
    CL Item
    Screening (Screening)
    C0220908 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Cycle 1 Day 1 (Cycle 1 Day 1)
    (Comment:en)
    CL Item
    Cycle 1 Day 8 (Cycle 1 Day 8)
    (Comment:en)
    CL Item
    Cycle 1 Day 15 (Cycle 1 Day 15)
    (Comment:en)
    CL Item
    Cycle 1 Day 22 (Cycle 1 Day 22)
    (Comment:en)
    CL Item
    Cycle 2 Day 1 (Cycle 2 Day 1)
    (Comment:en)
    CL Item
    Cycle 2 Day 8 (Cycle 2 Day 8)
    (Comment:en)
    CL Item
    Cycle 2 Day 15 (Cycle 2 Day 15)
    (Comment:en)
    CL Item
    Cycle 2 Day 22 (Cycle 2 Day 22)
    (Comment:en)
    CL Item
    Cycle 3 Day 1 (Cycle 3 Day 1)
    (Comment:en)
    CL Item
    Cycle 3 Day 8 (Cycle 3 Day 8)
    CL Item
    Cycle 3 Day 15 (Cycle 3 Day 15)
    CL Item
    Cycle 3 Day 22 (Cycle 3 Day 22)
    CL Item
    Interim Staging (Interim Staging)
    CL Item
    Cycle 4 Day 1 (Cycle 4 Day 1)
    CL Item
    Cycle 4 Day 8 (Cycle 4 Day 8)
    CL Item
    Cycle 4 Day 15 (Cycle 4 Day 15)
    CL Item
    Cycle 4 Day 22 (Cycle 4 Day 22)
    CL Item
    Cycle 5 Day 1 (Cycle 5 Day 1)
    CL Item
    Cycle 5 Day 8 (Cycle 5 Day 8)
    CL Item
    Cycle 5 Day 15 (Cycle 5 Day 15)
    CL Item
    Cycle 5 Day 22 (Cycle 5 Day 22)
    CL Item
    Cycle 6 Day 1 (Cycle 6 Day 1)
    CL Item
    Cycle 6 Day 8 (Cycle 6 Day 8)
    CL Item
    Cycle 6 Day 15 (Cycle 6 Day 15)
    CL Item
    Cycle 6 Day 22 (Cycle 6 Day 22)
    CL Item
    End of Treatment (End of Treatment)
    CL Item
    Follow Up 1: 3 months after EoT (Follow Up 1: 3 months after EoT)
    CL Item
    Follow Up 2: 6 months after EoT (Follow Up 2: 6 months after EoT)
    CL Item
    Follow Up 3: 9 months after EoT (Follow Up 3: 9 months after EoT)
    CL Item
    Follow Up 4: 12 months after EoT (Follow Up 4: 12 months after EoT)
    CL Item
    Follow Up 5: 15 months after EoT (Follow Up 5: 15 months after EoT)
    CL Item
    Follow Up 6: 18 months after EoT (Follow Up 6: 18 months after EoT)
    CL Item
    Follow Up 7: 21 months after EoT (Follow Up 7: 21 months after EoT)
    CL Item
    Follow Up 8: 24 months after EoT (Follow Up 8: 24 months after EoT)
    Item Group
    Vital signs
    C0518766 (UMLS CUI-1)
    Date
    Item
    Date
    date
    C0011008 (UMLS CUI [1])
    Blood Pressure Systolic
    Item
    Blood Pressure Systolic
    integer
    C0871470 (UMLS CUI [1])
    Blood Pressure Diastolic
    Item
    Blood Pressure Diastolic
    integer
    C0428883 (UMLS CUI [1])
    Pulse
    Item
    Pulse
    integer
    C0232117 (UMLS CUI [1])
    Body Temperature
    Item
    Body Temperature
    float
    C0005903 (UMLS CUI [1])
    ECOG
    Item
    ECOG
    integer
    C1520224 (UMLS CUI [1])
    Weight
    Item
    Weight
    float
    C0005910 (UMLS CUI [1])
    Height
    Item
    Height
    float
    C0005890 (UMLS CUI [1])
    Cycle day
    Item
    Cycle day not done
    boolean
    C0237753 (UMLS CUI [1,1])
    C0439228 (UMLS CUI [1,2])
    C0750729 (UMLS CUI [1,3])
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