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Intradermal booster COVID-19 vaccination

Safety and immunogenicity of intradermal and intramuscular booster COVID-19 vaccination following the 2-dose primary series of ChAdOx1(AstraZeneca) in Thai older people)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220112002
Enrollment
210
Registered
2022-01-12
Start date
2022-01-09
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

Intradermal mRNA-based vaccine following the 2-dose primary series of ChAdOx1 (AstraZeneca) can provide a sufficient level of immunity against SAR-CoV-2 booster vaccine, third dose, SAR-CoV2, older adult

Interventions

0.1 ml mRNA vaccine intradermal injection. Antibody levels are followed at 2-4 week and 12+/- weeks. Adverse event is followed for 7 days after injection ,0.3-0.5 ml mRNA vaccine intramuscular injecti
Experimental Biological/Vaccine,Active Comparator Biological/Vaccine

Sponsors

Faculty of Medicine Siriraj Hospital, Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 65 years old or more. 2. Having a 2-dose primary series of ChAdOx1 (AstraZeneca) vaccine for 12-24 weeks. 3. Stable and well-controlled chronic diseases. 4. Ability to understand and communicate in Thai language. 5. Ability to attend the appointment. 6.Ability to give informed consent

Exclusion criteria

Exclusion criteria: 1. Having a history of anaphylaxis to drug or other vaccines. 2. Having a previous history of Covid-19 infection or high-risk of Covid-19 infection. 3. Having any type of vaccination 2 week before the recruitment. 4. Having any type of immunodeficiency. 5. Taking any type of immunosuppressive agent or cytotoxic drug. 6. No acute illness or acute inflammation. 7. Having blood transfusion or other blood products, immunoglobulin, antiviral agent, or antibody within previous 90 days.

Design outcomes

Primary

MeasureTime frame
vaccine adverse event 7 days number of adverse event

Secondary

MeasureTime frame
SARSCov-2 IgG 1 day AU/ml,T cell response 1 day T cell Elispot,Neutralizing antibody assay, Focus reduction neutralization test 1 day percent foci reduction, inhibitory concentration at 50%

Countries

Thailand

Contacts

Public ContactPrasert Assantachai

Faculty of Medicine Siriraj Hospital, Mahidol University

prasert.uts@mahidol.ac.th66988323939

Outcome results

None listed

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