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Safety and Immunogenicity of an Inactivated Vaccine Against COVID-19 in Medical Workers

Safety and Immunogenicity of an Inactivated Vaccine Against COVID-19 in Medical Workers

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04795414
Enrollment
1370
Registered
2021-03-12
Start date
2021-01-14
Completion date
2023-01-31
Last updated
2021-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, SARS-CoV-2 Infection

Keywords

SARS-CoV-2, Covid19, Inactivated vaccine

Brief summary

With the unprecedented morbidity of the COVID-19 pandemic, the vaccine effectiveness needs to be assessed across diverse populations. The purpose of this study is to evaluate the safety and immunogenicity of an inactivated SARS-CoV-2 vaccine in medical workers.

Detailed description

1370 participants who were negative for serum-specific antibodies against SARS-CoV-2 at the time of screening were enrolled and were receive a two-dose schedule, 21 days apart, with 4 μg BBIBP-CorV inactivated SARS-CoV-2 vaccine. The primary safety outcome includes solicited local and systemic reactions prompted by and recorded in an electronic diary within 7 days post each injection, unsolicited adverse events and serious adverse events assessed from the receipt of each dose, and clinical laboratory abnormalities from dose 1 through 1month after dose 2. Laboratory tests included measurement of alanine aminotransferase, aspartate aminotransferase, serum total bilirubin, serum albumin, creatinine, blood urea nitrogen, and blood routine examination. Immunogenicity was assessed as the serum anti-SARS-CoV-2 specific antibody responses and neutralizing activity at 4 weeks after the second vaccination.

Interventions

BIOLOGICALSARS-CoV-2 Vaccine(Vero Cell), Inactivated

The subjects of Vaccination Group will receive two doses, 21 days apart of inactivated SARS-CoV-2 vaccine (4 μg of BBIBP-CorV)

Sponsors

Ruijin Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

* Written informed consent according to ICH/GCP regulations prior to any trial specific procedures. * Male or female aged 18-59 years.

Exclusion criteria

* NA

Design outcomes

Primary

MeasureTime frameDescription
Percentage of participants reporting local reactionswithin 7days post each vaccinationPain at the injection site, swelling, itch, and redness
Percentage of participants reporting systemic eventswithin 7days post each vaccinationFever, headache, fatigue, nausea, vomiting, diarrhea, constipation, myalgia, arthralgia
Percentage of participants reporting adverse eventsFrom Dose 1 through 1 month after Dose 2verified by investigators
Percentage of participants reporting serious adverse eventsFrom Dose 1 through 1 month after Dose 2verified by investigators
Serum anti-SARS-CoV-2 speicfic antibody and neutralizing antibody titresat 1 month after dose 2determination of anti-SARS-CoV-2 speicfic antibody and SARS-CoV-2 neutralizing antibody levels

Secondary

MeasureTime frameDescription
Serum anti-SARS-CoV-2 speicfic antibody and neutralizing antibody titresat 6 months after dose 2determination of anti-SARS-CoV-2 speicfic antibody and SARS-CoV-2 neutralizing antibody levels

Countries

China

Contacts

Primary ContactZhiTao Yang
yangzhitao@hotmail.fr+8613611965436
Backup ContactXiaoqi Yu
yuxiaoqi_03@163.com+8613817390935

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026