0 Ratings

ID

15692

Description

Nerventra Study (Eudra CT 2007-003226-19) Study MS-LAQ-301: A multinational, multicenter, randomized, double-blind, parallel-group, placebo-controlled study, to evaluate the safety, tolerability and efficacy of daily oral administration of laquinimod 0.6 mg in subjects with relapsing remitting multiple sclerosis (RRMS)

Keywords

  1. 6/8/16 6/8/16 -
Uploaded on

June 8, 2016

DOI

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License

Creative Commons BY-NC 3.0

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    Nerventra Study Laboratory data

    Nerventra Study Laboratory data

    Demographic Information
    Description

    Demographic Information

    Protocol Number
    Description

    Protocol Number

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C0008971
    UMLS CUI [1,2]
    C0600091
    Visit Type
    Description

    i.e "Screening"

    Data type

    text

    Alias
    UMLS CUI [1]
    C0545082
    Date of visit
    Description

    Visit date

    Data type

    date

    Alias
    UMLS CUI [1]
    C1320303
    Study site number
    Description

    Study site

    Data type

    integer

    Alias
    UMLS CUI [1]
    C2825164
    Subject number:
    Description

    Subject number

    Data type

    integer

    Alias
    UMLS CUI [1]
    C1709561
    No data to report
    Description

    Blank

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0750479
    Laboratory parameter
    Description

    Laboratory parameter

    Laboratory parameter
    Description

    Laboratory parameter

    Data type

    text

    Alias
    UMLS CUI [1]
    C0022885
    Date of laboratory test
    Description

    Date laboratory

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0022885
    Laboratory value
    Description

    Value

    Data type

    float

    Alias
    UMLS CUI [1]
    C0519835
    Unit
    Description

    Unit

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348328
    Normal range upper limit
    Description

    Normal range upper limit

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0086715
    UMLS CUI [1,2]
    C2827740
    Normal range lower limit
    Description

    Normal range lower limit

    Data type

    integer

    Alias
    UMLS CUI [1,1]
    C0086715
    UMLS CUI [1,2]
    C2827739

    Similar models

    Nerventra Study Laboratory data

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Demographic Information
    Protocol Number
    Item
    Protocol Number
    text
    C0008971 (UMLS CUI [1,1])
    C0600091 (UMLS CUI [1,2])
    Visit
    Item
    Visit Type
    text
    C0545082 (UMLS CUI [1])
    Visit date
    Item
    Date of visit
    date
    C1320303 (UMLS CUI [1])
    Study site
    Item
    Study site number
    integer
    C2825164 (UMLS CUI [1])
    Subject number
    Item
    Subject number:
    integer
    C1709561 (UMLS CUI [1])
    Blank
    Item
    No data to report
    boolean
    C0750479 (UMLS CUI [1])
    Item Group
    Laboratory parameter
    Laboratory parameter
    Item
    Laboratory parameter
    text
    C0022885 (UMLS CUI [1])
    Date laboratory
    Item
    Date of laboratory test
    date
    C0011008 (UMLS CUI [1,1])
    C0022885 (UMLS CUI [1,2])
    Value
    Item
    Laboratory value
    float
    C0519835 (UMLS CUI [1])
    Unit
    Item
    Unit
    text
    C2348328 (UMLS CUI [1])
    Normal range upper limit
    Item
    Normal range upper limit
    integer
    C0086715 (UMLS CUI [1,1])
    C2827740 (UMLS CUI [1,2])
    Normal range lower limit
    Item
    Normal range lower limit
    integer
    C0086715 (UMLS CUI [1,1])
    C2827739 (UMLS CUI [1,2])

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