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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | seasonal influenza vaccine | subjects 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.