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ID

33080

Descrizione

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

Keywords

  1. 26/11/18 26/11/18 -
Titolare del copyright

GSK group of companies

Caricato su

26 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

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

    Concomitant Medication Form

    Administrative data
    Descrizione

    Administrative data

    Subject Number
    Descrizione

    Subject Number

    Tipo di dati

    integer

    Concomitant Medication
    Descrizione

    Concomitant Medication

    Have any medications/treatments been administered during study period?
    Descrizione

    Have any medications/treatments been administered during study period?

    Tipo di dati

    boolean

    If Yes, please complete the following table
    Descrizione

    If Yes, please complete the following table

    Tipo di dati

    text

    List of Medications
    Descrizione

    List of Medications

    Trade/Generic Name
    Descrizione

    Trade/Generic Name

    Tipo di dati

    text

    Medical Indication
    Descrizione

    Medical Indication

    Tipo di dati

    text

    Total daily dose
    Descrizione

    Total daily dose

    Tipo di dati

    text

    Route
    Descrizione

    Route

    Tipo di dati

    text

    Start date
    Descrizione

    Start date

    Tipo di dati

    date

    End date
    Descrizione

    End date

    Tipo di dati

    date

    Ongoing at the end of study?
    Descrizione

    Ongoing at the end of study?

    Tipo di dati

    boolean

    Similar models

    Concomitant Medication Form

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Administrative data
    Subject Number
    Item
    Subject Number
    integer
    Item Group
    Concomitant Medication
    Have any medications/treatments been administered during study period?
    Item
    Have any medications/treatments been administered during study period?
    boolean
    If Yes, please complete the following table
    Item
    If Yes, please complete the following table
    text
    Item Group
    List of Medications
    Trade/Generic Name
    Item
    Trade/Generic Name
    text
    Item
    Medical Indication
    text
    Code List
    Medical Indication
    CL Item
    Prophylactic (1)
    Total daily dose
    Item
    Total daily dose
    text
    Route
    Item
    Route
    text
    Start date
    Item
    Start date
    date
    End date
    Item
    End date
    date
    Ongoing at the end of study?
    Item
    Ongoing at the end of study?
    boolean

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