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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | In this study, a probiotic lozenge formulation containing S. salivarius K12, M18 and prebiotic will be evaluated for its potential to improve bad breath | In 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. |
| OTHER | Placebo | Probiotic 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.