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This study is undertaken to evaluate the effectiveness of currently licensed varicella vaccines under conditions of routine use in a setting where varicella vaccine is included in the childhood immunization calendar.
Observational, multicenter, population-based, matched case-control study conducted in selected pediatric practices in the Munich area.
Age
1 - No limit years
Sex
ALL
Healthy Volunteers
Yes
GSK Investigational Site
Baldham, Bavaria, Germany
GSK Investigational Site
Deisenhofen, Bavaria, Germany
GSK Investigational Site
Freising, Bavaria, Germany
GSK Investigational Site
Fürstenfeldbruck, Bavaria, Germany
GSK Investigational Site
Gilching, Bavaria, Germany
GSK Investigational Site
Grafing, Bavaria, Germany
GSK Investigational Site
Grafrath, Bavaria, Germany
GSK Investigational Site
Kirchheim, Bavaria, Germany
GSK Investigational Site
Munich, Bavaria, Germany
GSK Investigational Site
Munich, Bavaria, Germany
Start Date
February 1, 2008
Primary Completion Date
October 1, 2010
Completion Date
October 1, 2010
Last Updated
October 29, 2012
1,012
ACTUAL participants
Varicella (chickenpox) lesion sampling
PROCEDURE
Lead Sponsor
GlaxoSmithKline
Collaborators
NCT07475000
NCT06891872
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT00226499