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ID

33097

Beschrijving

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

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Versies (1)
  1. 27-11-18 27-11-18 -
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GSK group of companies

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27 november 2018

DOI

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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

    Engels

    Diary Card: Local Symptoms - Dose 2

    1 Formulieren  
    Administrative data
    Beschrijving

    Administrative data

    Dose Number
    Beschrijving

    Dose Number

    Datatype

    text

    Subject Number
    Beschrijving

    Subject Number

    Datatype

    integer

    Local Symptoms (at injection site)
    Beschrijving

    Local Symptoms (at injection site)

    please fill in below and assess the occurrence of any of the following signs or symptoms according to the criteria listed hereafter
    Beschrijving

    please fill in below and assess the occurrence of any of the following signs or symptoms according to the criteria listed hereafter

    Datatype

    text

    Local Symptoms
    Beschrijving

    Local Symptoms

    Day
    Beschrijving

    Day

    Datatype

    integer

    Redness
    Beschrijving

    size

    Datatype

    float

    Maateenheden
    • mm
    mm
    Swelling
    Beschrijving

    size

    Datatype

    float

    Maateenheden
    • mm
    mm
    Pain
    Beschrijving

    intensity; please measure the greatest diameter

    Datatype

    text

    Ongoing after Day 3?
    Beschrijving

    Ongoing after Day 3?

    Datatype

    boolean

    If Yes, record the date of last day of symptoms
    Beschrijving

    If Yes, record the date of last day of symptoms

    Datatype

    date

    Local Symptoms (Group Priorix)
    Beschrijving

    Local Symptoms (Group Priorix)

    Day
    Beschrijving

    Day

    Datatype

    integer

    Redness
    Beschrijving

    size

    Datatype

    float

    Maateenheden
    • mm
    mm
    Swelling
    Beschrijving

    size

    Datatype

    float

    Maateenheden
    • mm
    mm
    Pain
    Beschrijving

    intensity

    Datatype

    integer

    Ongoing after Day 3
    Beschrijving

    Ongoing after Day 3

    Datatype

    boolean

    If Yes, date of last day of symptoms
    Beschrijving

    If Yes, date of last day of symptoms

    Datatype

    date

    for investigator only (Priorix vaccine)
    Beschrijving

    for investigator only (Priorix vaccine)

    Side
    Beschrijving

    Side

    Datatype

    text

    Site
    Beschrijving

    Site

    Datatype

    text

    Local Symptoms (Group Varilrix)
    Beschrijving

    Local Symptoms (Group Varilrix)

    Day
    Beschrijving

    Day

    Datatype

    integer

    Redness
    Beschrijving

    size

    Datatype

    float

    Maateenheden
    • mm
    mm
    Swelling
    Beschrijving

    size

    Datatype

    float

    Maateenheden
    • mm
    mm
    Pain
    Beschrijving

    intensity

    Datatype

    integer

    Ongoing after day 3?
    Beschrijving

    Ongoing after day 3?

    Datatype

    boolean

    If Yes, record the date of last day of symptoms
    Beschrijving

    If Yes, record the date of last day of symptoms

    Datatype

    date

    for investigator only (Varilrix vaccine)
    Beschrijving

    for investigator only (Varilrix vaccine)

    Side
    Beschrijving

    Side

    Datatype

    integer

    Site
    Beschrijving

    Site

    Datatype

    integer

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    Similar models

    Diary Card: Local Symptoms - Dose 2

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Administrative data
    Item
    Dose Number
    text
    Dose Number
    Code List
    Dose Number
    CL Item
    Dose 2 (1)
    Subject Number
    Item
    Subject Number
    integer
    Item Group
    Local Symptoms (at injection site)
    please fill in below and assess the occurrence of any of the following signs or symptoms according to the criteria listed hereafter
    Item
    please fill in below and assess the occurrence of any of the following signs or symptoms according to the criteria listed hereafter
    text
    Item Group
    Local Symptoms
    Item
    Day
    integer
    Day
    Code List
    Day
    CL Item
    Day 0 (1)
    CL Item
    Day 1 (Evening) (2)
    CL Item
    Day 2 (Evening) (3)
    CL Item
    Day 3 (Evening) (4)
    Redness
    Item
    Redness
    float
    Swelling
    Item
    Swelling
    float
    Item
    Pain
    text
    Pain
    Code List
    Pain
    CL Item
    Absent (1)
    CL Item
    Minor reaction to touch (2)
    CL Item
    Cries/protests on touch (3)
    CL Item
    Cries when limb is moved/spontaneously painful (4)
    Ongoing after Day 3?
    Item
    Ongoing after Day 3?
    boolean
    If Yes, record the date of last day of symptoms
    Item
    If Yes, record the date of last day of symptoms
    date
    Item Group
    Local Symptoms (Group Priorix)
    Item
    Day
    integer
    Day
    Code List
    Day
    CL Item
    Day 0 (1)
    CL Item
    Day 1 (Evening) (2)
    CL Item
    Day 2 (Evening) (3)
    CL Item
    Day 3 (Evening) (4)
    Redness
    Item
    Redness
    float
    Swelling
    Item
    Swelling
    float
    Item
    Pain
    integer
    Pain
    Code List
    Pain
    CL Item
    Absent (1)
    CL Item
    Minor reaction to touch (2)
    CL Item
    Cries/protests on touch (3)
    CL Item
    Cries when limb is moved/spontaneously painful (4)
    Ongoing after Day 3
    Item
    Ongoing after Day 3
    boolean
    If Yes, date of last day of symptoms
    Item
    If Yes, date of last day of symptoms
    date
    Item Group
    for investigator only (Priorix vaccine)
    Item
    Side
    text
    Side
    Code List
    Side
    CL Item
    Upper left (1)
    CL Item
    Lower left (2)
    CL Item
    Upper right (3)
    CL Item
    Lower right (4)
    Item
    Site
    text
    Site
    Code List
    Site
    CL Item
    Arm (1)
    CL Item
    Thigh (2)
    CL Item
    Buttock (3)
    Item Group
    Local Symptoms (Group Varilrix)
    Item
    Day
    integer
    Day
    Code List
    Day
    CL Item
    Day 0 (1)
    CL Item
    Day 1 (Evening) (2)
    CL Item
    Day 2 (Evening) (3)
    CL Item
    Day 3 (Evening) (4)
    Redness
    Item
    Redness
    float
    Swelling
    Item
    Swelling
    float
    Item
    Pain
    integer
    Pain
    Code List
    Pain
    CL Item
    Absent (1)
    CL Item
    Minor reaction to touch (2)
    CL Item
    Cries/protests on touch (3)
    CL Item
    Cries when limb is moved/spontaneously painful (4)
    Ongoing after day 3?
    Item
    Ongoing after day 3?
    boolean
    If Yes, record the date of last day of symptoms
    Item
    If Yes, record the date of last day of symptoms
    date
    Item Group
    for investigator only (Varilrix vaccine)
    Item
    Side
    integer
    Side
    Code List
    Side
    CL Item
    Upper left (1)
    CL Item
    Lower left (2)
    CL Item
    Upper right (3)
    CL Item
    Lower right (4)
    Item
    Site
    integer
    Site
    Code List
    Site
    CL Item
    Arm (1)
    CL Item
    Thigh (2)
    CL Item
    Buttock (3)
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