Yongping Center for Diseases Control and Prevention
Dali, Yunnan, 650022, China
NCT Number: NCT04992208
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 3~17 years and in people with pre-existing disease to provide reference for improving the immunization strategy of COVID-19 vaccine.
Looking for future studies?
Notify Me3 year–17 year
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 3~17 years . 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 August 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 33000 subjects including patients with pre-existing will be enrolled with 3000 for each research center, including 600 subjects aged 3~5years,1200 subjects aged 6~11 years,1200 subjects aged 12~17 years.
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 aluminium hydroxide solution per injection
Other names: CoronaVac
Time frame: Within 0~7 days after each dose
Incidence rate of adverse reactions within 0~7 days after each dose in all populations.
Time frame: Within 0-28 days after each dose vaccination
Incidence rate of adverse reactions within 0~28 days after each dose in all populations
Time frame: Within 0~7 days after each dose vaccination
Incidence of adverse reactions within 0~7 days after each dose in each age group
Time frame: Within 0~28 days after each dose vaccination
Incidence rate of adverse reactions within 0~28 days after each dose in each age group
Time frame: Within 0~7 days after each dose vaccination
Incidence of adverse reactions within 0~7 days after each dose in the population with pre-existing disease.
Time frame: Within 0~28 days after each dose vaccination
Incidence of adverse reactions within 0~28 days after each dose in the population with pre-existing disease.
Sinovac Life Sciences Co., Ltd.
Industry
Safety Observation of the Inactivated SARS-CoV-2 Vaccine (Vero Cell) in Population Aged 3~17 Years : A Multicenter,Open-label Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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.
Published trials that share one or more normalized conditions with this study.
NCT04794829
COVID-19, Coronaviridae Infections
Bethesda, Maryland, United States
View Trial DetailsNCT07552779
COVID-19, COVID-19 (Coronavirus Disease 2019)
Brussels, Bruxelles-capitale, Région de, Belgium
View Trial DetailsNCT07722000
COVID-19, Chronic Disease
Banī Suwayf, Beni Suweif Governorate, Egypt
View Trial DetailsNCT04371432
COVID-19, Coronaviridae Infections
Bethesda, Maryland, United States
View Trial Details