A Post-marketing Safety Study of Inactivated, Split-virion Influenza Vaccine in Subjects Aged 3 Years and Older
NCT ID: NCT02133456
Last Updated: 2014-05-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
166240 participants
OBSERVATIONAL
2014-01-31
2014-04-30
Brief Summary
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The hypothesis is that there is no significant difference in the occurrence of adverse events among influenza vaccines manufactured by SIBP and other companies.
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Detailed Description
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Adverse events were collected through the Adverse Events Following Immunization (AEFI) Surveillance System. Beijing CDC and local prefectural CDC must organize an expert panel to investigate adverse events and assess causality, using criteria based on Chinese Standard Procedures for Vaccination. The panels consist of physicians, epidemiologists, pharmacists, and other relevant experts. In general, expert panels investigate deaths, life-threatening illnesses, and permanent disabilities, and immunization-program managers or vaccination providers investigate common, minor adverse events. Adverse events are classified into one of five categories: vaccine reactions (common and minor to rare and more serious), program errors, coincidental illnesses, psychogenic reactions, and unclassifiable events.
At the time of vaccination, vaccinees were instructed to report any adverse event to physicians or vaccination providers. The following adverse events were required to be reported: adverse events that were fatal or that resulted in disability and clusters of events (i.e., notably high numbers of similar adverse events related to a certain vaccine) ; anaphylaxis or other allergic reactions occurring within 24 hours after vaccination; fever (axillary temperature, \>37.5°C), angioedema, or a local injection-site reaction (diameter, \>2.5 cm) occurring within 5 days after vaccination; purpura, an Arthus reaction, febrile convulsion, seizure, or polyneuritis occurring within 15 days after vaccination; and the Guillain-Barré syndrome occurring within 3 months after vaccination. Other reactions that were common and minor (e.g., mild pain and fatigue) were not required to be reported.
Conditions
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Study Design
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ECOLOGIC_OR_COMMUNITY
Study Groups
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SIBP's vaccine
SIBP's vaccine group is the population injected with this vaccine.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Recipients of SIBP's inactivated, split-virion influenza vaccine.
Exclusion Criteria
* Receipt of a live vaccine within 4 weeks prior to Study Day 1.
* Any condition, which in the opinion of the study doctor, might interfere with the evaluation of the study objective.
3 Years
ALL
Yes
Sponsors
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Shanghai Institute Of Biological Products
INDUSTRY
Centers for Disease Control and Prevention, China
OTHER_GOV
Responsible Party
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Wu Jiang
Department of Immunization and Prevention,Beijing Centers for Disease Control and Prevention
Principal Investigators
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Jiang Wu, Master
Role: PRINCIPAL_INVESTIGATOR
Beijing Centers for Disease Prevention and Control, China
Other Identifiers
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BJCDCWJ201401
Identifier Type: -
Identifier Source: org_study_id
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