Evaluation of Immunogenicity of COVID-19 Vaccine in Chinese Population
1 other identifier
observational
100
1 country
1
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 15, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2024
CompletedFirst Submitted
Initial submission to the registry
November 21, 2024
CompletedFirst Posted
Study publicly available on registry
January 8, 2025
CompletedJanuary 8, 2025
November 1, 2024
8 months
November 21, 2024
January 7, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
PBMC
When 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.
About two and a half years
Study Arms (1)
Observation
Interventions
Eligibility Criteria
People infected with COVID-19
You may qualify if:
- He was infected with COVID-19 from November to December 2022;
- Have not been infected with COVID-19 (the subject said that he was not infected and signed the informed consent form);
- Those who agree and sign the informed consent form.
You may not qualify if:
- Missing or incomplete questionnaires that affect research results;
- Individuals with combined dysfunction of important organs such as the heart, liver, and lungs;
- Mental and behavioral abnormalities;
- Intellectual disability;
- Under 18 years old or over 75 years old;
- Low understanding and communication skills.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Xijing Hospitallead
Study Sites (1)
The First Affiliated Hospital of Air Force Military Medical University
Xi'an, Shaanxi, 710004, China
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 21, 2024
First Posted
January 8, 2025
Study Start
November 15, 2023
Primary Completion
June 30, 2024
Study Completion
June 30, 2024
Last Updated
January 8, 2025
Record last verified: 2024-11