drugset / Trial / NCT00138385

Comparison of Inactivated and Live, Attenuated Influenza Vaccine in Children 5-9 Years of Age-Year 3 Amendment

NCT00138385

RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate how young children's bodies learn to fight against flu infection and to see how vaccines may help to fight against the flu. This is a Phase 4, single-center, randomized study of the immune responses of 40 children, ages 5-9, given one of two licensed influenza vaccines (either inactivated vaccine given in an arm muscle or live, attenuated vaccine inhaled through the nose). Study procedures will include up to 3 blood samples. Participants will complete a diary to document any side effects experienced following the vaccination. Participants will return to the clinic for a visit on Day 7-9 and again 4-6 weeks following vaccination. Participants that have not been previously vaccinated will receive a 2nd dose of vaccine. A follow up telephone call will occur 8-10 weeks following vaccination. Total study participation will be up to 75 days.

Timeline

Start
2005-08
Primary completion
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject FluMist Vaccine 0.25 ml Intranasal
Subject Influenza Virus Vaccine Vaccine 0.5 ml Intramuscular

Indications