Clinical Trials Directory

Trials / Completed

CompletedNCT01906190

Persistence of Immune Response After Vaccination With Influenza Vaccine

Persistence Study of Immune Response After Vaccination With Influenza Vaccine in Healthy Population

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
207 (actual)
Sponsor
Centers for Disease Control and Prevention, China · Other Government
Sex
All
Age
12 Years – 60 Years
Healthy volunteers
Accepted

Summary

This clinical study will be performed in subjects aged 12-60 years old enrolled in NCT01310374 who received 2010 seasonal influenza vaccine to evaluate the persistence of the immune response of influenza vaccine up to 24 months after vaccination.

Detailed description

Subjects were previously vaccinated at 12 to 60 years of age with 2010 seasonal influenza vaccine.The persistence phase starts 24 months after the primary vaccination and blood samples will be taken at 6, 12, 18 and 24 months after primary vaccination. Subjects whose antibody titer less than 1:40 at 6 months after primary vaccination will receive a booster dose of influenza vaccine.

Conditions

Interventions

TypeNameDescription
BIOLOGICALseasonal influenza vaccinesubjects whose antibodies less than 1:40 6 months later after primary vaccination will receive a booster dose of seasonal influenza vaccine

Timeline

Start date
2011-08-01
Primary completion
2013-03-01
Completion
2013-07-01
First posted
2013-07-24
Last updated
2013-07-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01906190. Inclusion in this directory is not an endorsement.

Persistence of Immune Response After Vaccination With Influenza Vaccine (NCT01906190) · Clinical Trials Directory