drugset / Trial / NCT00115531

Eldery High Dose TIV 2005

NCT00115531

RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to compare a new higher-dose influenza virus vaccine to the standard dose vaccine in elderly adults who can walk. Current influenza vaccines protect elderly against viral influenza but not as well as desired. It is expected that the higher doses vaccine can be given with little reaction, but this needs to be tested. Up to 410 people ages 65 years and older will be recruited from the community and from existing volunteer populations. Participants will receive either the high or standard dose injected in the muscle, remain in the clinic for 20 minutes afterward, and maintain a daily memory aid for 7 days. The memory aid will be reviewed by telephone 8-12 days after the injection and return to the clinic or contacted by telephone 6 months after the injection.

Timeline

Start
2005-04
Primary completion
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Influenza Virus Vaccine Vaccine 45 ug Intramuscular
Subject Influenza Virus Vaccine Vaccine 180 ug Intramuscular

Indications