0 Évaluations
ID

35806

Description

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

Mots-clés

Versions (2)
  1. 25/03/2019 25/03/2019 -
  2. 25/03/2019 25/03/2019 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

25 mars 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

  • Plus récent
  • Plus ancien
  • Favori
  • Plus récent
    • Plus récent
    • Plus ancien
    • Favori

    Aucun commentaire

    Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

    GSK Biologicals' Hib-MenCY-TT Conjugate Vaccine vs ActHIB® & MenC Conjugate Licensed Vaccine (NCT00134719)

    Anglais

    Concomitant Vaccination

    1 Formulaires  
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Number
    Description

    Clinical Trial Subject Unique Identifier

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Concomitant Vaccination
    Description

    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 ?
    Description

    Vaccination, Concomitant Agent

    Type de données

    text

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

    Vaccination, Concomitant Agent, Medication name

    Type de données

    text

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

    Vaccination, Concomitant Agent, Drug Administration Routes

    Type de données

    text

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

    Vaccination, Concomitant Agent, Administration procedure, Date in time

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0042196
    UMLS CUI [1,2]
    C2347852
    UMLS CUI [1,3]
    C1533734
    UMLS CUI [1,4]
    C0011008
    Retour au début de la page

    Similar models

    Concomitant Vaccination

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    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])
    Retour au début de la page 

    Aide

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial