World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: EUCTR
Last refreshed on: 19 March 2012
Main ID:  EUCTR2007-000298-49-FR
Date of registration: 23/01/2007
Prospective Registration: Yes
Primary sponsor: CHU - Hôpitaux de Rouen
Public title: EVALUATION DE LA REPONSE IMMUNITAIRE CONTRE LA SOUCHE DE NEISSERIA MENINGITIDIS B:14,P1.7,16 CHEZ LES SUJETS VACCINES PAR MenBVac - Immunogénicité MenBVac
Scientific title: EVALUATION DE LA REPONSE IMMUNITAIRE CONTRE LA SOUCHE DE NEISSERIA MENINGITIDIS B:14,P1.7,16 CHEZ LES SUJETS VACCINES PAR MenBVac - Immunogénicité MenBVac
Date of first enrolment: 02/02/2007
Target sample size: 0
Recruitment status: Authorised-recruitment may be ongoing or finished
URL:  https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2007-000298-49
Study type:  Interventional clinical trial of medicinal product
Study design:  Controlled: no Randomised: no Open: no Single blind: no Double blind: no Parallel group: no Cross over: no Other: no Other trial design description: prospectif If controlled, specify comparator, Other Medicinial Product: no Placebo: Other:  
Phase: 
Countries of recruitment
France
Contacts
Name:    
Address: 
Telephone:
Email:
Affiliation: 
Name:    
Address: 
Telephone:
Email:
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria:
1) enfant demeurant dans la zone de Dieppe (canton de Dieppe-Est, canton de Dieppe-Ouest, canton d'Offranville) nés entre le 01/01/2000 et le 23/06/2005 et déjà vaccinés par 2 doses de MenBVac.

2) consentement éclairé délivré par le(s) titulaire(s) de l'autorité parentale.
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion criteria:
1) impossibilité d'obtenir le consentement de tous les titulaires de l'autorité parentale,

2) impossibilité de réaliser les prélèvements sanguins avant la troisième dose vaccinale,

3) impossibilité d'effectuer la 3e dose vaccinale de MenBVac


Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes
Health Condition(s) or Problem(s) studied
SUJETS VACCINES PAR MenBVac.
Intervention(s)

Product Name: MenBVac
Pharmaceutical Form: Solution for injection

Primary Outcome(s)
Secondary Objective: none
Main Objective: L' objectif est l'estimation du pourcentage des enfants de la zone de Dieppe, vaccinés par MenBvac, ayant un titre d'activité bactéricide du sérum vis-à-vis du clone de N. meningitidis B:14,P1-7,16 réputé corrélé à la protection (=4 ) avant et après la 3ème dose de MenBvac® .
Primary end point(s): 1°) Titrage de l'activité bactéricide du sérum vis à vis d'une souche de N. meningitidis du clone B:14,P1-7, 16 représentative des souches responsables d'infections méningococciques invasives survenues à Dieppes.
Secondary Outcome(s)
Secondary ID(s)
2007/004/HP
Source(s) of Monetary Support
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history