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Immunological Responses and safety after COVID-19 vaccination in Healthcare Workers at Siriraj Hospital, Bangkok

Immunological Responses and safety after COVID-19 vaccination in Healthcare Workers at Siriraj Hospital, Bangkok

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210720002
Enrollment
360
Registered
2021-07-20
Start date
2021-03-25
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

healthy volunteers healthcare Workers

Interventions

Participant received viral vector vaccine will be checked the antibody level at baseline before the first dose vaccination, before second dose, 4 weeks, 24 weeks and 48 weeks after complete vaccinatio
Experimental Biological/Vaccine,Active Comparator Biological/Vaccine
Viral vector vaccine,Inactivated vaccine

Sponsors

Faculty of Medicine Siriraj Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Males or females at least 18 years of age (inclusive) 2. Be subject of study Seroprevalence, Incidence and Immunological Responses to SARS-CoV-2 Infection among Frontline Healthcare Workers compare with Non-COVID-19 HCWs during the COVID-19 Pandemic at Siriraj Hospital, Bangkok or healthcare workers who interested in receiving the vaccine in the study 3. Capable of informed consent and provision of written informed consent before any study procedures

Exclusion criteria

Exclusion criteria: 1. Could not receive vaccine such as history of anaphylaxis or severe infection with high temperature (over 38C) 2. Have received blood transfusion, plasma, blood product, blood components, immunoglobulins, antiviral or antibodies for treatment of COVID-19 within the last 90 days - Have detected COVID-19 infection within the last 10 days 3. Have unstable disease or could not control the symptom such as chest pain, dyspnea, palpitation, etc. 4. Be pregnant 5. Have history of immunodeficiency or use immunosuppressant

Design outcomes

Primary

MeasureTime frame
Adverse events 48 week Proportion of participant with adverse events within 7 days after vaccination

Secondary

MeasureTime frame
Level of antibody response 48 week IgG level

Countries

Thailand

Contacts

Public ContactNasikarn Angkasekwinai

Mahidol University

nasikarn.ang@mahidol.ac.th0818708766

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026