Yongping Center for Diseases Control and Prevention
Dali, Yunnan, 650022, China
NCT Number: NCT04911790
This study is a multi-center and open design, phase Ⅳ clinical trial of an inactivated SARS-CoV-2 vaccine (CoronaVac) manufactured by Sinovac Research and Development Co., Ltd.The purpose of this study is to evaluate the safety of the SARS-CoV-2 Inactivated vaccine in population aged 18 years years and older and in people with pre-existing disease to provide reference for improving the immunization strategy of COVID-19 vaccine.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Dali, Yunnan, 650022, China
This study is a multi-center and open design, phase Ⅳ clinical trial in population aged 18 years years and older. The experimental vaccine will be manufactured by Sinovac Research and Development Co.,Ltd.The study is planned to be carried out in 11 provinces from May 2021 to December 2022, including Liaoning, Heilongjiang, Anhui, Fujian, Jiangxi, Hubei, Guangxi, Chongqing, Guizhou, Yunnan and Gansu. Each province will serve as a research center, and each research center will select the corresponding research site.A total of 121000 subjects will be enrolled with11000 for each research center, including at least 2000 people with pre-existing disease and at least 4000 people in the elderly group (60 years old and above) (including patients with pre-existing disease).And subjects will receive two doses of vaccine on day 0 and day 28.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
SARS-CoV-2 Inactivated Vaccine 600SU inactivated virus in 0·5 mL of aluminiumhydroxide solution per injection
Other names: CoronaVac
Time frame: Day 0-7 after each dose vaccination
Incidence rate of adverse reactions within 0~7 days after each dose in all populations.
Time frame: Day 0-7 after each dose vaccination
Incidence of adverse reactions within 0~7 days after each dose in the population with pre-existing disease.
Time frame: Day 0-28 after each dose vaccination
Incidence rate of adverse reactions within 0~28 days after each dose in all populations.
Time frame: Day 0-28 after each dose vaccination
Incidence of adverse reactions within 0~28 days after each dose in the population with pre-existing disease.
Sinovac Research and Development Co., Ltd.
Industry
Safety Observation of the Inactivated SARS-CoV-2 Vaccine (Vero Cell) in Population Aged 18 Years and Older: A Multicenter,Open-label Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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