To further characterize the immune responses induced after an influenza vaccination performed either via the ID or the IM routes in two clearly distinct populations. Objectives: * To describe the immune response per age group and vaccine group after vaccination. * To describe the safety of the vaccines per age group and per vaccine group after vaccination.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
160
0.1 mL, Intradermal
0.5 mL, Intramuscular
0.1 mL, Intradermal
Unnamed facility
Lyon Sud, France
To provide information concerning immune response to an inactivated, split-virion, influenza vaccine.
Time frame: 21 days post-vaccination
To provide information concerning the safety of inactivated, split-virion, influenza vaccine.
Time frame: 21 days post-vaccination and entire study duration
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0.5 mL, Intramuscular