Assessing the immunological responses and adverse reactions elicited by the heterologous second booster dose of BNT162b2 after two-dose CoronaVac for COVID-19 vaccination COVID-19
Conditions
Interventions
The heterologous second booster dose of BNT162b2 after two-dose CoronaVac for COVID-19 vaccination in healthcare workers of Faculty of Medicine, Naresuan University.
Experimental Biological/Vaccine
the heterologous second booster dose of BNT162b2 after two-dose CoronaVac for COVID-19 vaccination
Sponsors
The National Science Research and Innovation Fund
Naresuan University
Eligibility
Sex/Gender
All
Age
20 Years to No maximum
Inclusion criteria
Inclusion criteria: 20 years old or older who never had prior clinical symptoms of SARS-CoV-2 infection.
Exclusion criteria
Exclusion criteria: immunocompromised persons, receiving immunosuppressive drugs, receiving blood products and pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The IgG against the SARS-CoV-2-spike protein 4 and 24 weeks after the second booster dose of BNT162b2. fluoroenzymeimmunoassay | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse reactions at the first 3 days, 4 weeks and 24 weeks after the second booster dose of BNT162b2. Case record form | — |
Countries
Thailand
Contacts
Public ContactSupawadee Makanut
Faculty of Medicine, Naresuan University
Outcome results
None listed