ID

25951

Beskrivning

Investigators Statement Ropinirole Case Report Form GSK Study ID: 100013 Clinical Study ID: RRL100013 A 12-Week, Double-Blind, Placebo-Controlled, Twice-Daily Dosing Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Requiring Extended Treatment Coverage

Nyckelord

  1. 2017-10-01 2017-10-01 -
Rättsinnehavare

gsk

Uppladdad den

1 oktober 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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    Investigators Statement Ropinirole Case Report Form GSK RRL100013

    Investigators Statement Ropinirole Case Report Form GSK RRL100013

    INVESTIGATOR’S STATEMENT
    Beskrivning

    INVESTIGATOR’S STATEMENT

    Alias
    UMLS CUI-1
    C1710187
    UMLS CUI-2
    C2826892
    Subject number
    Beskrivning

    Subject number

    Datatyp

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Check all Adverse Event forms are up to date and complete
    Beskrivning

    Adverse Event

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0877248
    Check that the Concomitant Medication form is up to date
    Beskrivning

    Concomitant Medication

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Check that all appropriate pages are signed (thus indicating completion) and dated
    Beskrivning

    completion

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0805732
    Check that laboratory results are included
    Beskrivning

    laboratory results

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1254595
    I certify to the best of my knowledge, that the observations and findings are recorded correctly and completely in this CRF.
    Beskrivning

    consent

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1511481
    Investigator
    Beskrivning

    Investigator

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2826892
    Date:
    Beskrivning

    Date

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C0011008

    Similar models

    Investigators Statement Ropinirole Case Report Form GSK RRL100013

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    INVESTIGATOR’S STATEMENT
    C1710187 (UMLS CUI-1)
    C2826892 (UMLS CUI-2)
    Subject number
    Item
    Subject number
    integer
    C2348585 (UMLS CUI [1])
    Adverse Event
    Item
    Check all Adverse Event forms are up to date and complete
    boolean
    C0877248 (UMLS CUI [1])
    Concomitant Medication
    Item
    Check that the Concomitant Medication form is up to date
    boolean
    C2347852 (UMLS CUI [1])
    completion
    Item
    Check that all appropriate pages are signed (thus indicating completion) and dated
    boolean
    C0805732 (UMLS CUI [1])
    laboratory results
    Item
    Check that laboratory results are included
    boolean
    C1254595 (UMLS CUI [1])
    consent
    Item
    I certify to the best of my knowledge, that the observations and findings are recorded correctly and completely in this CRF.
    boolean
    C1511481 (UMLS CUI [1])
    Investigator
    Item
    Investigator
    text
    C2826892 (UMLS CUI [1])
    Date
    Item
    Date:
    date
    C0011008 (UMLS CUI [1])

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