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ID

15684

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)

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Versions (1)
  1. 6/8/16 6/8/16 -
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June 8, 2016

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Creative Commons BY-NC 3.0
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    Nerventra Study Medication log

    English

    Nerventra Study Medication log

    1 forms  
    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
    Medication log
    Description

    Medication log

    Date of automatic update
    Description

    Date of automatic update

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0205554
    UMLS CUI [1,3]
    C1519814
    Date of manual update
    Description

    Date of manual update

    Data type

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0175674
    UMLS CUI [1,3]
    C1519814
    Medication name,ongoing
    Description

    Medication name

    Data type

    text

    Alias
    UMLS CUI [1,1]
    C2360065
    UMLS CUI [1,2]
    C0549178
    Visit Type
    Description

    Visit

    Data type

    text

    Alias
    UMLS CUI [1]
    C0545082
    Concomitant medications log
    Description

    Concomitant medications log

    Medication name
    Description

    Medication name

    Data type

    text

    Alias
    UMLS CUI [1]
    C2360065
    Start date
    Description

    Concomitant Medication Start Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C2826734
    End Date
    Description

    Concomitant Medication End Date

    Data type

    date

    Alias
    UMLS CUI [1]
    C2826744
    Ongoing
    Description

    Concomitant Medication Ongoing

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    Concomitant medication use indication
    Description

    Indication

    Data type

    text

    Alias
    UMLS CUI [1]
    C2826696
    Total daily dose
    Description

    Total daily dose

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348070
    Unit of dosage
    Description

    Unit

    Data type

    text

    Alias
    UMLS CUI [1]
    C2348328
    Medication frequency
    Description

    Medication frequency

    Data type

    text

    Alias
    UMLS CUI [1]
    C3476109
    Route of administration
    Description

    Route of administration

    Data type

    text

    Alias
    UMLS CUI [1]
    C0013153
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    Similar models

    Nerventra Study Medication log

    1 forms
    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
    Medication log
    Date of automatic update
    Item
    Date of automatic update
    date
    C0011008 (UMLS CUI [1,1])
    C0205554 (UMLS CUI [1,2])
    C1519814 (UMLS CUI [1,3])
    Date of manual update
    Item
    Date of manual update
    date
    C0011008 (UMLS CUI [1,1])
    C0175674 (UMLS CUI [1,2])
    C1519814 (UMLS CUI [1,3])
    Medication name
    Item
    Medication name,ongoing
    text
    C2360065 (UMLS CUI [1,1])
    C0549178 (UMLS CUI [1,2])
    Visit
    Item
    Visit Type
    text
    C0545082 (UMLS CUI [1])
    Item Group
    Concomitant medications log
    Medication name
    Item
    Medication name
    text
    C2360065 (UMLS CUI [1])
    Concomitant Medication Start Date
    Item
    Start date
    date
    C2826734 (UMLS CUI [1])
    Concomitant Medication End Date
    Item
    End Date
    date
    C2826744 (UMLS CUI [1])
    Concomitant Medication Ongoing
    Item
    Ongoing
    boolean
    C2826666 (UMLS CUI [1])
    Indication
    Item
    Concomitant medication use indication
    text
    C2826696 (UMLS CUI [1])
    Total daily dose
    Item
    Total daily dose
    text
    C2348070 (UMLS CUI [1])
    Unit
    Item
    Unit of dosage
    text
    C2348328 (UMLS CUI [1])
    Medication frequency
    Item
    Medication frequency
    text
    C3476109 (UMLS CUI [1])
    Route of administration
    Item
    Route of administration
    text
    C0013153 (UMLS CUI [1])
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