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OpenTrials
Completed

NCT Number: NCT04992208

Safety of an Inactivated SARS-CoV-2 Vaccine for Prevention of COVID-19 in Children and Adolescents

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.

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Key information

Age range

3 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Yongping Center for Diseases Control and Prevention

Dali, Yunnan, 650022, China

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have not received any COVID-19 vaccine in the past or at least one dose of CoronaVac manufactured by Sinovac Research and Development Co.,Ltd;
  • Population aged 3~17 years ;
  • The subjects can understand and voluntarily sign the informed consent form and participate in the follow-up;

Exclusion criteria

  • History of severe allergy to the vaccine such as acute allergic reaction,angioedema and dyspnea ;
  • Severe neurological disease such as Myelitis transverse,Guillain-Barre Syndrome and demyelinating disorders;
  • Acute disease,acute onset of chronic disease and severe chronic diseases.

Treatment and study plan

Experimental Group

Biological

SARS-CoV-2 Inactivated Vaccine 600SU inactivated virus in 0·5 mL of aluminium hydroxide solution per injection

Other names: CoronaVac

Primary outcomes

  1. Safety index 1-incidence of adverse reactions

    Time frame: Within 0~7 days after each dose

    Incidence rate of adverse reactions within 0~7 days after each dose in all populations.

Secondary outcomes

  1. Safety index 2-incidence of adverse reactions

    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

  2. Safety index 3-incidence of adverse reactions

    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

  3. Safety index 4-incidence of adverse reactions

    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

  4. Safety index 5-incidence of adverse reactions

    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.

  5. Safety index 6-incidence of adverse reactions

    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.

Sponsors and collaborators

Lead sponsor

Sinovac Life Sciences Co., Ltd.

Industry

Registry information

Official study title

Safety Observation of the Inactivated SARS-CoV-2 Vaccine (Vero Cell) in Population Aged 3~17 Years : A Multicenter,Open-label Study

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Aug 5, 2021
Registry last updated
Sep 25, 2023

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.

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