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Clinical Trial Summary

The aim of this study is to monitor any impact in the change from the lyophilised formulation to the liquid formulation of the Rotarix™ vaccine on hospitalisations for rotavirus gastroenteritis. This is planned to be assessed by comparing trends of hospitalisations due to laboratory confirmed rotavirus gastroenteritis in children <=5 years of age, before and after introduction of the liquid formulation of the vaccine in Belgium.


Clinical Trial Description

n/a


Study Design

Observational Model: Ecologic or Community, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT01435967
Study type Observational
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date September 2011
Completion date September 2014

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