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Trials / Not Yet Recruiting

Not Yet RecruitingNCT07384130

Oral Probiotics for Halitosis in Healthy Adults

Efficacy of Oral Probiotics on Cysteine-Induced Halitosis in Healthy Adult Volunteers.

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
John Hale · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to evaluate efficacy of a probiotic lozenge containing BLIS M18, BLIS K12 and a prebiotic in healthy adults.

Detailed description

This is a double-blind, randomized controlled colonization pilot study with no crossover to evaluate the efficacy of probiotic lozenges on halitosis in healthy adults. Participants will be randomly assigned to 2 groups consuming probiotic lozenge containing Streptococcus salivarius M18 and K12 and with prebiotic over a 13 day period. Breath scores will be measured at predetermined time points pre and post intervention.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTIn this study, a probiotic lozenge formulation containing S. salivarius K12, M18 and prebiotic will be evaluated for its potential to improve bad breathIn this study, a probiotic-free lozenge formulation containing S. salivarius K12, M18 and prebiotic will be evaluated for its potential to improve bad breath as a comparator.
OTHERPlaceboProbiotic free placebo lozenge

Timeline

Start date
2026-03-15
Primary completion
2026-06-15
Completion
2026-07-15
First posted
2026-02-03
Last updated
2026-02-04

Locations

1 site across 1 country: New Zealand

Source: ClinicalTrials.gov record NCT07384130. Inclusion in this directory is not an endorsement.