CTRI/2022/01/039677尚未招募3 期
Interventional study to determine efficacy, safety and immunogenicity of booster dose of ChAdOx1 nCoV-19 (COVISHIELD) Coronavirus Disease (COVID-19) vaccine in vaccine recipients.- A single centre, randomised control trial - COVIBOOST
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Healthy volunteers above 18 years who have received 2 doses of ChAdOx1 nCoV-19 vaccine
- •Able and willing to comply with study requirements
- •Willing to refrain from blood donation during the study period
- •giving consent
排除标准
- •Anaphylactic reaction following administration of vaccine previously
- •Pregnant or lactating women
- •Any adverse event that in the opinion of the Investigator may affect the safety of the participant or the interpretation of the study results
- •Subject not giving consent
- •Individuals who have received any other COVID1-9 vaccine
研究者
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