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Clinical Trial Summary

To determine if prophylactic supplementation with B. lactis HN019 reduces the risk of developing physician- and laboratory-confirmed influenza infection at any time during the 12-week supplementation period.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01258842
Study type Interventional
Source Fonterra Research Centre
Contact Tisha Golden
Email tisha.golden@sprim.com
Status Recruiting
Phase Phase 3
Start date December 2010
Completion date May 2011

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