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Clinical Trial Summary

The aim of this study is to test saliva samples obtained from healthy human participants for anti-viral activity after they have consumed S. salivarius probiotic in a powder format.


Clinical Trial Description

This is a randomized controlled open pilot study to evaluate saliva samples collected from participants following their consumption of powders containing the commercially marketed probiotic bacterium S. salivarius K12 or S. salivarius M18. Participants will be randomly assigned to one of the 4 groups consuming probiotic powder containing Streptococcus salivarius K12 or S. salivarius M18 with or without prebiotics (e.g. sugars that may promote probiotic activity). Saliva samples will be collected at predetermined time points pre and post intervention. Antibacterial and Antiviral activity will be determined following established assays. Colonisation efficacy will be determined by enumerating the probiotic in the saliva samples using standard microbiological techniques. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05374070
Study type Interventional
Source BLIS Technologies Limited
Contact John D Hale, PhD
Phone 6434740988
Email john.hale@blis.co.nz
Status Recruiting
Phase N/A
Start date May 23, 2022
Completion date August 15, 2022

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