Clinical Trial

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

Study acronym: VaQDENV
Recruiting
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Summary
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-01-14.
Status change: Not Yet Recruiting → Recruiting 2025-05-16
Trial Details
NCT Number NCT06776692
Lead Sponsor IRCCS Sacro Cuore Don Calabria di Negrar
Conditions Dengue Vaccines
Enrollment 402 participants
Start Date 2024-07-10
Primary Completion 2028-01 (estimated)
Study Completion 2028-01 (estimated)
Updated on ClinicalTrials.gov 2025-05-18