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Evaluation of Immunogenicity of COVID-19 Vaccine in Chinese Population

Evaluation of Immunogenicity of COVID-19 Vaccine in Chinese Population

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06763887
Enrollment
100
Registered
2025-01-08
Start date
2023-11-15
Completion date
2024-06-30
Last updated
2025-01-08

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

Conditions

COVID

Brief summary

The purpose of this study is to evaluate the immunogenicity and immune protection of COVID-19, especially the recently prevalent strains, against the background of current immunization in Chinese population

Interventions

OTHERNo Interventions

No intervention

Sponsors

Xijing Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. He was infected with COVID-19 from November to December 2022; 2. Have not been infected with COVID-19 (the subject said that he was not infected and signed the informed consent form); 3. Those who agree and sign the informed consent form.

Exclusion criteria

1. Missing or incomplete questionnaires that affect research results; 2. Individuals with combined dysfunction of important organs such as the heart, liver, and lungs; 3. Mental and behavioral abnormalities; 4. Intellectual disability; 5. Under 18 years old or over 75 years old; 6. Low understanding and communication skills.

Design outcomes

Primary

MeasureTime frameDescription
PBMCAbout two and a half yearsWhen conducting blood sample analysis, we focus on separating and evaluating in detail the composition and counting of peripheral blood mononuclear cell (PBMC). This process involves identifying and quantifying various types of mononuclear cells in the sample, such as lymphocytes, monocytes, etc. These cells are crucial for understanding an individual's immune status. Through precise separation techniques and advanced cell analysis methods, we are able to obtain accurate and detailed reports on the classification and quantity of mononuclear cells.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026