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Immunological responses and adverse reactions of the heterologous second booster dose of BNT162b2 after two-dose CoronaVac for COVID-19 vaccination in healthcare workers of Faculty of Medicine, Naresuan University.

Phase 3
Recruiting
Conditions
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
SAR-CoV-2 second booster dose
heterologous vaccination
BNT162b2
CoronaVac
healthcare workers
Registration Number
TCTR20221112001
Lead Sponsor
The National Science Research and Innovation Fund
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
340
Inclusion Criteria

20 years old or older who never had prior clinical symptoms of SARS-CoV-2 infection.

Exclusion Criteria

immunocompromised persons, receiving immunosuppressive drugs, receiving blood products and pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The IgG against the SARS-CoV-2-spike protein 4 and 24 weeks after the second booster dose of BNT162b2. fluoroenzymeimmunoassay
Secondary Outcome Measures
NameTimeMethod
Adverse reactions at the first 3 days, 4 weeks and 24 weeks after the second booster dose of BNT162b2. Case record form
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