drugset / Trial / NCT00504231

Intradermal Influenza Vaccine Study in Elders

NCT00504231

RandomizedParallel-groupOpen-labelPrevention

Summary

This randomized trial compared the immunogenicity of 60% dose intradermal (ID) influenza vaccination to standard intramuscular (IM) vaccination of full-dose or 60% dose vaccine. Pre- and postvaccination measurements in the hemagglutination inhibition antibody (HAI) titer were compared. Participants who received reduced-dose vaccine were revaccinated with full-dose IM vaccine.

Timeline

Start
2007-09
Primary completion
2008-01
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Influenza Virus Vaccine Vaccine 0.15 ml Intravenous
Subject Influenza Virus Vaccine Vaccine 0.3 ml Intravenous
Subject Influenza Virus Vaccine Vaccine 0.5 ml Intravenous

Indications