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ID

33068

Description

Study ID: 104020 Clinical Study ID: 104020 Study Title: Blinded, randomised study to assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ live attenuated measles-mumps-rubella-varicella candidate vaccine when given to healthy children in their second year of life Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00126997 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Combined Measles, Mumps, Rubella, Varicella Vaccine Trade Name: Priorix Tetra Study Indication: Measles; Mumps; Rubella; Varicella CRF Seiten: 268-336; 870-938

Keywords

  1. 11/26/18 11/26/18 -
Copyright Holder

GSK group of companies

Uploaded on

November 26, 2018

DOI

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License

Creative Commons BY-NC 3.0

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    Immunogenicity of Combined Measles, Mumps, Rubella, Varicella Vaccine for healthy 2 y.o children - 104020

    Febrile Convulsions AE Form

    Administrative data
    Description

    Administrative data

    Subject Number
    Description

    Subject Number

    Data type

    integer

    Febrile Convulsions - Suspected Signs of Meningitis
    Description

    Febrile Convulsions - Suspected Signs of Meningitis

    Event Number
    Description

    Please report any febrile convulsion and any suspected signs of meningitis occurring during the study period

    Data type

    integer

    Description
    Description

    Description

    Data type

    text

    Further Details (For GSK)
    Description

    Further Details (For GSK)

    Event Number
    Description

    Event Number

    Data type

    text

    Date started
    Description

    Date started

    Data type

    date

    Date stopped
    Description

    Date stopped

    Data type

    date

    Intensity
    Description

    Intensity

    Data type

    text

    Was a neurological examination performed?
    Description

    Was a neurological examination performed?

    Data type

    boolean

    If Yes, was a lumbar puncture performed?
    Description

    If Yes, was a lumbar puncture performed?

    Data type

    boolean

    If Yes, date of exam
    Description

    If Yes, date of exam

    Data type

    date

    Relationship to investigational products
    Description

    Relationship to investigational products

    Data type

    boolean

    Outcome
    Description

    Outcome

    Data type

    text

    Similar models

    Febrile Convulsions AE Form

    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    Administrative data
    Subject Number
    Item
    Subject Number
    integer
    Item Group
    Febrile Convulsions - Suspected Signs of Meningitis
    Item
    Event Number
    integer
    Code List
    Event Number
    CL Item
    FC. 1 (1)
    CL Item
    FC. 2 (2)
    Description
    Item
    Description
    text
    Item Group
    Further Details (For GSK)
    Item
    Event Number
    text
    Code List
    Event Number
    CL Item
    FC. 1 (1)
    CL Item
    FC. 2 (2)
    Date started
    Item
    Date started
    date
    Date stopped
    Item
    Date stopped
    date
    Item
    Intensity
    text
    Code List
    Intensity
    CL Item
    Mild (1)
    CL Item
    Moderate (2)
    CL Item
    Severe (3)
    Was a neurological examination performed?
    Item
    Was a neurological examination performed?
    boolean
    If Yes, was a lumbar puncture performed?
    Item
    If Yes, was a lumbar puncture performed?
    boolean
    If Yes, date of exam
    Item
    If Yes, date of exam
    date
    Relationship to investigational products
    Item
    Relationship to investigational products
    boolean
    Item
    Outcome
    text
    Code List
    Outcome
    CL Item
    Recovered/resolved (1)
    CL Item
    Recovering/resolving (2)
    CL Item
    Not recovered/not resolved (3)
    CL Item
    Recovered with sequelae/resolved with sequelae (4)

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