Clinical Trials Directory

Trials / Unknown

UnknownNCT05204602

Safety and Immunogenicity of COVID-19 Vaccine Booster in Patients With Liver Diseases

Safety and Immunogenicity of Third Dose SARS-CoV-2 Vaccine Booster in Patients With Liver Diseases Following Two Doses of Inactivated Vaccines (NMCID-CHESS 2201): a Multicenter Cohort Study

Status
Unknown
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Huashan Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Previous studies should that patients with chronic liver diseases, cirrhosis, hepatocellular carcinoma and post-liver-trasplant status had lower immunological response to SARS-CoV-2 vaccines than healthy population. Along with the waning of antibody and emerging SARS-CoV-2 variants, a third dose SARS-CoV-2 booster vaccination is now considered as an effective strategy. Previous studies showed good safety and immunogenicity of the SARS-CoV-2 booster vaccination in healthy population. However, the relevant information in patients with liver diseases need further research. This study (NMCID-CHESS 2201) aimed to investigate the safety and immunogenicity of the SARS-CoV-2 booster vaccination in population with chronic liver diseases

Conditions

Timeline

Start date
2022-02-10
Primary completion
2022-08-20
Completion
2022-12-20
First posted
2022-01-24
Last updated
2022-02-14

Locations

19 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05204602. Inclusion in this directory is not an endorsement.

Safety and Immunogenicity of COVID-19 Vaccine Booster in Patients With Liver Diseases (NCT05204602) · Clinical Trials Directory