A Surveillance Study of Diseases Specified as Adverse Events of Special Interest, of Other Adverse Events Leading to Hospitalisation or Death, and of Meningitis in Children in Africa Prior to Implementation of the RTS,S/AS01E Candidate Vaccine

CompletedOBSERVATIONAL
Enrollment

36,366

Participants

Timeline

Start Date

October 5, 2015

Primary Completion Date

August 2, 2022

Study Completion Date

August 2, 2022

Conditions
Malaria
Interventions
PROCEDURE

Blood collection

For all hospitalised children suspected of having an AESI or meningitis, a sample of 5 ml of whole blood was collected and the serum was stored.

Trial Locations (5)

40102

GSK Investigational Site, Kisumu

Unknown

GSK Investigational Site, Ouagadougou

GSK Investigational Site, PO BOX 02 Nouna

GSK Investigational Site, Kintampo

GSK Investigational Site, Navrongo

Sponsors
All Listed Sponsors
collaborator

PATH

OTHER

collaborator

Agence de Médecine Préventive, France

OTHER

collaborator

Réseau en Afrique Francophone pour la Télémédecine,

OTHER

collaborator

Iqvia Pty Ltd

INDUSTRY

collaborator

Parexel

INDUSTRY

collaborator

Clinical Laboratory Services

OTHER

lead

GlaxoSmithKline

INDUSTRY