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ID

35806

Beschrijving

Study ID: 102370 (primary study) Clinical Study ID: 102370 Study Title: A multicentre when given according to the 2-4-6 month schedule to healthy infants with booster dose at 12 to 15 months Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00134719 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Haemophilus influenzae Type b, Meningococcal C and Y-Tetanus Toxoid Conjugate Vaccine Trade Name: BIO HIB-MENCY-TT; MenHibrix Study Indication: Haemophilus influenzae type b; Neisseria Meningitidis

Trefwoorden

Versies (2)
  1. 25-03-19 25-03-19 -
  2. 25-03-19 25-03-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

25 maart 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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    GSK Biologicals' Hib-MenCY-TT Conjugate Vaccine vs ActHIB® & MenC Conjugate Licensed Vaccine (NCT00134719)

    Engels

    Concomitant Vaccination

    1 Formulieren  
    Administrative Data
    Beschrijving

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Beschrijving

    Clinical Trial Subject Unique Identifier

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Concomitant Vaccination
    Beschrijving

    Concomitant Vaccination

    Alias
    UMLS CUI-1
    C0042196
    UMLS CUI-2
    C2347852
    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol ?
    Beschrijving

    Vaccination, Concomitant Agent

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0042196
    UMLS CUI [1,2]
    C2347852
    Trade / (Generic) Name
    Beschrijving

    Vaccination, Concomitant Agent, Medication name

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0042196
    UMLS CUI [1,2]
    C2347852
    UMLS CUI [1,3]
    C2360065
    Route
    Beschrijving

    Vaccination, Concomitant Agent, Drug Administration Routes

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0042196
    UMLS CUI [1,2]
    C2347852
    UMLS CUI [1,3]
    C0013153
    Administration date
    Beschrijving

    Vaccination, Concomitant Agent, Administration procedure, Date in time

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C0042196
    UMLS CUI [1,2]
    C2347852
    UMLS CUI [1,3]
    C1533734
    UMLS CUI [1,4]
    C0011008
    Terug naar het begin van de pagina

    Similar models

    Concomitant Vaccination

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Number
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Concomitant Vaccination
    C0042196 (UMLS CUI-1)
    C2347852 (UMLS CUI-2)
    Item
    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol ?
    text
    C0042196 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    Vaccination, Concomitant Agent
    Code List
    Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol ?
    CL Item
    No (1)
    CL Item
    Yes, please record concomitant vaccination with trade name and / or generic name, route and vaccine administration date. (2)
    Vaccination, Concomitant Agent, Medication name
    Item
    Trade / (Generic) Name
    text
    C0042196 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    C2360065 (UMLS CUI [1,3])
    Vaccination, Concomitant Agent, Drug Administration Routes
    Item
    Route
    text
    C0042196 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    C0013153 (UMLS CUI [1,3])
    Vaccination, Concomitant Agent, Administration procedure, Date in time
    Item
    Administration date
    date
    C0042196 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    C1533734 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    Terug naar het begin van de pagina 

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