SWITCH ON: Analysing the Immunogenicity of Additional Booster Vaccinations in HCW

NCT05471440 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 431

Last updated 2023-02-15

No results posted yet for this study

Summary

Eighty percent of the Dutch population has completed a primary COVID-19 vaccination regimen, and 60% of the population received a booster vaccination. Waning immunity, combined with the emergence of antigenically distinct SARS-CoV-2 variants, has led to the consideration of additional booster vaccinations in the Dutch population by autumn 2022. However, despite efforts of the Dutch policymakers, the public's willingness to repeatedly receive COVID-19 booster vaccinations is declining. This is mainly due to a reduced burden of disease by COVID-19, fewer hospitalizations, and fewer deaths. However, population immunity might be one of the major factors responsible for this reduced burden of disease, possibly emphasizing the need for booster vaccinations. In this proposal we will address an important question asked by policymakers: "Are booster vaccinations in autumn recommended for the healthy population?"

Conditions

  • Covid-19 Vaccination

Interventions

DRUG

Direct boost mRNA

Participants will be boosted with a covid-19 vaccin after priming with mRNA

DRUG

Direct boost adeno

Participants will be boosted with a covid-19 vaccin after priming with adeno

DRUG

Post-poned boost mRNA

Participants will be boosted with a covid-19 vaccin after priming with mRNA

DRUG

Post-poned boost adeno

Participants will be boosted with a covid-19 vaccin after priming with adeno

Sponsors & Collaborators

  • ZonMw: The Netherlands Organisation for Health Research and Development

    collaborator OTHER
  • Leiden University Medical Center

    collaborator OTHER
  • University Medical Center Groningen

    collaborator OTHER
  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    collaborator OTHER
  • Erasmus Medical Center

    lead OTHER

Principal Investigators

  • Hugo van der Kuy, PharmD · Erasmus MC, Rotterdam

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
67 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-08-20
Primary Completion
2022-09-15
Completion
2023-08-30

Countries

  • Netherlands

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 NCT05471440 on ClinicalTrials.gov