Colonisation Efficacy of Oral Probiotic Fast Melt Powder

Status Recruiting

Clinical Trial Summary

To evaluate the colonisation efficacy (i.e. ability of the probiotic bacteria to remain in your mouth) of a fast melt powder that quickly dissolves in the mouth. The fast melt powder will contain a Streptococcus salivarius probiotic and the study is to be done in healthy adults.

Clinical Trial Description

This is a double-blind, randomized controlled study with no cross over to evaluate the colonization efficacy of fast melt powders containing a commercially available probiotic bacterium Streptococcus salivarius K12. Participants will be randomly assigned to one of the 2 groups consuming Fast Melt powder containing two different doses of Streptococcus salivarius K12 over a seven day period. Saliva samples will be collected at predetermined time points pre and post intervention. Colonization efficacy will be determined by enumerating the probiotic in the saliva samples using standard microbiological techniques. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05367518
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 15, 2022
Completion date	June 30, 2022

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