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Clinical Trial Summary

This pilot study, to be conducted in the 2017/2018 influenza season, is a safety surveillance study using passive surveillance enhanced with a reporting card system to report adverse events of interest (AEIs) after Flu vaccination.


Clinical Trial Description

This is the third pilot study following, EPI-FLU-045 VS UK [NCT02567721] and EPI-FLU-046 VS UK [NCT02893878] studies, carried out in the 2 previous influenza seasons (2015/2016 and 2016/2017). This study will collect data about vaccination status and adverse events following influenza immunisation (AEFI) on a weekly basis, from 01 September 2017 onwards, using a customized Adverse Drug Reaction (ADR) Cards and data from Electronic Health Records system for a period of approximately 13 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03278067
Study type Observational
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date September 12, 2017
Completion date November 30, 2017

See also
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