ID

23881

Descripción

Study part: Informed consent Visit 1. A phase 2 study to assess safety, reactogenicity and immunogenicity of a booster dose of an investigational vaccination regimen and GSK Biologicals Hib-MenC vaccine (co-administered with Infanrix penta) compared to a booster dose of Menjugate (co-administered with Infanrix hexa).Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Study ID: 100381, Clinical Study ID: 100381

Palabras clave

  1. 16/7/17 16/7/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

16 de julio de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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Informed consent Visit 1 Hib-MenCY-TT-004 BST 003 Neisseria Meningitidis-Haemophilus influenzae type b Vaccine 100381

Informed consent Visit 1

INFORMED CONSENT
Descripción

INFORMED CONSENT

Alias
UMLS CUI-1
C0021430
Date of visit
Descripción

Date of visit

Tipo de datos

date

Alias
UMLS CUI [1]
C1320303
Subject Number
Descripción

Subject Number

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
I certify that Informed Consent has been obtained prior to any study procedure.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Informed Consent Date :
Descripción

Informed Consent Date

Tipo de datos

date

Alias
UMLS CUI [1]
C2985782

Similar models

Informed consent Visit 1

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
INFORMED CONSENT
C0021430 (UMLS CUI-1)
Date of visit
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Subject Number
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
Informed Consent
Item
I certify that Informed Consent has been obtained prior to any study procedure.
boolean
C0021430 (UMLS CUI [1])
Informed Consent Date
Item
Informed Consent Date :
date
C2985782 (UMLS CUI [1])

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