COVID-19 Vaccines Safety Tracking (CoVaST)

NCT04834869 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 30000

Last updated 2022-04-06

No results posted yet for this study

Summary

This project aims to monitor the side effects of COVID-19 vaccines worldwide actively. The primary objectives of the project include a) to estimate the prevalence of each local and systemic side effect of each COVID-19 vaccine among healthcare workers (HCW), old adults over +65 (OA), and schoolteachers (ST); b) to evaluate the potential demographic and medical risk factors for side effects frequency and intensity; c) to evaluate the long-term consequences of COVID-19 vaccines. The secondary objectives include a) to evaluate the relative safety of COVID-19 vaccines compared to each other; b) to evaluate the impact of palliative drugs used by the recently vaccinated individuals on their short-term side effects resolution.

Conditions

  • Adverse Reaction to Vaccine
  • COVID19 Vaccine

Interventions

BIOLOGICAL

BNT162b2

Receiving either the first dose only or both doses of BNT162b2 vaccine (Pfizer-BioNTech COVID-19 Vaccine)

BIOLOGICAL

mRNA-1273

Receiving either the first dose only or both doses of mRNA-1273 vaccine (Moderna COVID-19 Vaccine)

BIOLOGICAL

AZD1222

Receiving either the first dose only or both doses of AZD1222 vaccine (AstraZeneca-Oxford University COVID-19 Vaccine)

BIOLOGICAL

CoronaVac

Receiving either the first dose only or both doses of CoronaVac (Sinovac COVID-19 Vaccine)

BIOLOGICAL

Sinopharm

Receiving either the first dose only or both doses of Sinopharm Vero Cell COVID-19 Vaccine

BIOLOGICAL

Gam-COVID-Vac

Receiving either the first dose only or both doses of Gam-COVID-Vac (Sputnik V)

BIOLOGICAL

JNJ-78436735

Receiving JNJ-78436735 (Janssen COVID-19 Vaccine)

BIOLOGICAL

CVnCoV

Receiving either the first dose only or both doses of CVnCoV (CureVac COVID-19 vaccine)

BIOLOGICAL

NVX-CoV2373

Receiving either the first dose only or both doses of NVX-CoV2373 (Novavax COVID-19 vaccine)

BIOLOGICAL

BBV152

Receiving either the first dose only or both doses of BBV152 (Covaxin COVID-19 vaccine)

Sponsors & Collaborators

  • Masaryk University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2025-12-31
Completion
2026-12-31
FDA Drug
Yes

Countries

  • United States
  • Canada
  • Croatia
  • Czechia
  • Estonia
  • Ethiopia
  • Germany
  • Ghana
  • Mexico
  • Poland
  • Portugal
  • Russia
  • Serbia
  • Slovenia

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04834869 on ClinicalTrials.gov