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A Study to Evaluate Vaccines Against COVID-19 in the Real World

H

Humanity & Health Medical Group Limited

Status

Withdrawn

Conditions

Hepatic Carcinoma
Chronic Liver Disease

Study type

Observational

Funder types

Other

Identifiers

NCT04775056
APASL_COVID-19 Vaccine_Ab

Details and patient eligibility

About

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the resulting coronavirus disease 2019 (COVID-19) have afflicted tens of millions of people in a worldwide pandemic. Considering its high mortality and rapid spread, an effective vaccine is urgently needed to control this pandemic. Recently, mass vaccination campaigns using newly approved vaccines, ranging from conventional viral and protein-based vaccines to those that are more cutting edge, including DNA- and mRNA-based vaccines are beginning in many parts of the world. Randomized clinical trials of different vaccines reported efficacies for preventing COVID-19 in the range of 50% to 95%.

Although these randomized clinical trials are considered the "gold standard" for evaluating intervention effects, they have notable limitations of sample size and subgroup analysis, restrictive inclusion criteria, and a highly controlled setting that may not be replicated in a mass vaccine rollout.

The aim of this study is to evaluate the safety, tolerability, immunogenicity, and efficacy of different vaccines against COVID-19 under real-world practice conditions.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects received COVID-19 vaccines;
  • Able to comprehend and provide written informed consent in accordance with institutional guidelines.

Exclusion criteria

  • Not received any COVID-19 vaccines;
  • Not willing to participate and/or give their written informed consent.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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