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Characterisation of Dengue Vaccine-induced Specific Immunity in Vaccinees With and Without Prior Exposure to Flavivirus Infections or Vaccination

Recruitingn/aAges 4 Years - anyAllIRCCS Sacro Cuore Don Calabria di Negrar
NCT06776692 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this observational study is to learn about the immunity induced by the Qdenga® vaccine in vaccinees. Participants that will receive the Dengue vaccine as part of their routine before a travel will be asked to undergo a blood sample at the time of administration of the first dose (T0), 24-48 hours after the first dose (T1) of the vaccine, immediately before the second dose (T2 ) and one to two months after the second dose (T3). Possibly a further sample will be collected within 2 years.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Subjects of both sexes presenting to the DITM to receive the anti-DENV vaccine whether or not they have had a history of prior DENV or other flaviviruses infection or a history of prior vaccination against other flaviviruses. These data will be recorded in the study CRF. * Age \>= 4 years. * Signed informed consent. Exclusion Criteria: * Age \< 4 years. * Absence of signed informed consent.
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What it tests

  • Qdenga
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Where

1 site
IRCCS Sacro Cuore Don Calabria
Negrar, Italy
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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