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About
The purpose of this study is to determine the efficacy of the liquid formulation of CAIVT against culture confirmed influenza illness in healthy children aged at least 6 months and less than 36 months, attending day care centers in Europe. In addition, the trial provides the opportunity to investigate the effect of CAIV-T on acute otitis media, on healthcare resource utilization and economic resources.
Enrollment
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Inclusion criteria
Exclusion criteria
Note: A pregnant household member is not considered a contraindication to enrollment.
Primary purpose
Allocation
Interventional model
Masking
2,903 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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