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Evaluation of neutralizing antibody titers and persistence of immune effects after the third dose of novel coronavirus inactivated vaccine

Evaluation of neutralizing antibody titers and persistence of immune effects after the third dose of novel coronavirus inactivated vaccine

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059259
Enrollment
Unknown
Registered
2022-04-27
Start date
2021-10-20
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Evaluation of the effectiveness and persistence of immune effects after COVID-19 vaccination

Interventions

Experimental group:None

Sponsors

Zhuhai People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The age is between 18 and 59; 2. Two inoculations of domestic COVID-19 inactivated vaccine have been completed, and the interval between the second dose of vaccine is more than 6 months; 3. Good compliance and voluntary signing of informed consent.

Exclusion criteria

Exclusion criteria: 1. The history of novel coronavirus infection; 2. Have a history of allergy to drugs or vaccines; 3. Respiratory symptoms such as fever, runny nose and cough have occurred in the past 7 days; 4. There has been a history of high and medium risk areas or overseas living in the past 14 days; 5. Vaccination history of other types of COVID-19 vaccines except domestic inactivated COVID-19 vaccines; 6. Patients with cardiovascular and cerebrovascular diseases, malignant tumors, gastrointestinal diseases, acute and chronic kidney diseases, infectious diseases or serious mental and neurological diseases; 7. Patients with immune deficiency or immunosuppression treatment; 8. Being involved in other COVID-19 related clinical trials or other drug clinical trials; 9. According to the judgment of the researcher, the subject has any other factors that are not suitable for the clinical trial.

Design outcomes

Primary

MeasureTime frame
Serum neutralizing antibody titer and immune level;

Countries

China

Contacts

Public ContactMeixiao Zhan

Zhuhai People's Hospital

zhanmeixiao1987@126.com+86 15989069680

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026