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N/A N=193 Randomized Basic Science

Immune Responses Induced by Different Licensed Influenza Vaccines

Immune Response

Enrolled (actual)
193
Serious AEs
0.0%
Results posted
Nov 2017
Primary outcome: Primary: T Cell Responses Following Immunization — 1.5; 1.7; 1.9; 1.6 fold change

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Flulaval (Biological); Fluvirin (Biological); Fluzone (Biological); Fluarix (Biological); Afluria (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Massachusetts, Worcester
Primary completion
Apr 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
T Cell Responses Following Immunization
1.5; 1.7; 1.9; 1.6; 2.4; 2.1
SECONDARY
Antibody Responses Following Immunization
7.32; 7.02; 5.71; 5.26; 7.6; 7.2

Summary

The goal of this research is to find out how the body's immune system responds to different manufacturer's "flu" vaccines.

Eligibility Criteria

Inclusion Criteria

  • Adults (18-50 years of age)
  • Willing to donate a blood sample multiple times
  • Willing to sign informed consent and HIPAA

Exclusion Criteria

  • Known systemic hypersensitivity reactions to egg proteins (eggs or egg products), to chicken proteins
  • Known hypersensitivity to neomycin, thimerosol (mercury derivative), neomycin, or polymyxin
  • Previous life threatening reaction to influenza vaccine
  • Individuals with altered immunocompetence state from medical condition ( HIV, cancer) or through immunosuppressive therapy(irradiation,corticosteroids, antimetabolites, alkylating agents, cytotoxic agents)
  • Occurrence of neurological syndrome within six weeks of previous influenza immunization
  • Active neurological disorder characterized by changing neurological disorder
  • Pregnancy
  • Acute febrile illness
  • History of anemia or bleeding disorders
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00902278). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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