Actively Recruiting
Efficacy of SALI-10 Oral Probiotics in Experimental Gingivitis
Led by Ostia Sciences · Updated on 2025-12-01
60
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
Sponsors
O
Ostia Sciences
Lead Sponsor
U
University of Toronto
Collaborating Sponsor
AI-Summary
What this Trial Is About
Gingivitis is among the most prevalent oral diseases worldwide, affecting an estimated 50-90% of adults. It is a reversible condition primarily caused by microbial plaque accumulation on teeth and gingival surfaces, which triggers inflammation. Standard care emphasizes plaque reduction through oral hygiene, and research shows gingivitis can be reversed once hygiene resumes. The classic experimental gingivitis (EG) model developed in 1965 by Löe and Silness demonstrated the direct link between plaque buildup and gingival inflammation, further confirming that gingival health can be restored after resuming proper care. Microbial ecology shifts are central to gingivitis pathogenesis. In health, the oral microbiome is dominated by gram-positive Streptococcus species. With plaque accumulation, microbial communities transition to gram-negative periopathogens such as Porphyromonas, Tannerella, Treponema, and Prevotella. This dysbiosis provokes heightened inflammation, tissue damage, and, in susceptible individuals, progression to periodontitis. Individual variability in the inflammatory response has been associated with differences in the presence and activity of beneficial streptococci. Certain strains of Streptococcus salivarius produce lantibiotics called salivaricins-polycyclic antimicrobial peptides containing lanthionine residues. Salivaricins inhibit oral pathogens and have been investigated for their antimicrobial and probiotic properties, particularly in the context of rising antibiotic resistance. Probiotic S. salivarius strains isolated from healthy individuals have demonstrated safety and antimicrobial potential in previous studies, supporting their use in preventing oral and respiratory infections. A strain of S. salivarius designated SALI-10 produces a lantibiotic, Salivaricin 10, and is being evaluated as a candidate for gingivitis prevention. This strain is hypothesized to (1) help stabilize populations of beneficial streptococci during plaque accumulation, (2) competitively inhibit periopathogens such as Porphyromonas and Prevotella, and (3) suppress the dysbiotic shift toward gram-negative dominance. By contributing to microbial balance and reducing inflammatory triggers, SALI-10 may support resilient host-microbe interactions associated with gingival health. This approach may offer a dual antimicrobial and microbiome-stabilizing strategy with relevance to gingivitis management and longer-term periodontal health.
CONDITIONS
Official Title
Efficacy of SALI-10 Oral Probiotics in Experimental Gingivitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female volunteers aged 18 to 70 years
- In good general health, classified as ASA I
- No signs of gingival inflammation at more than 90% of sites examined
- No periodontal pockets; probing depth less than 3.0 mm on all teeth/sites
- No clinical attachment loss (0 mm)
- No history of periodontal disease
- At least 20 gradeable teeth present
- Non-smokers
- Fluent in English
- For participants of childbearing potential, use at least one effective birth control method such as abstinence, hormonal birth control, intrauterine devices, confirmed vasectomy, or condoms
You will not qualify if you...
- Presence of orthodontic bands
- Use of partial or full dentures
- Tumors in soft or hard oral tissues
- Cavitated tooth decay requiring immediate treatment
- Allergy to personal care or dentifrice ingredients
- Participation in another clinical study within one month before this study
- Medical condition requiring pre-medication before dental visits
- Current or recent use (within 30 days) of antibiotics, anti-inflammatory, or antimicrobial drugs
- History of periodontal disease
- History of systemic inflammatory, immune, or immunocompromised conditions
- Pregnant or breastfeeding, or planning pregnancy
- Use of tobacco products
- Long-term antibiotic or anti-inflammatory therapy
- Use of medications or natural health products affecting gums (e.g., calcium channel blockers, anti-epileptic therapy)
- Any medical condition or medication that may affect safety or study quality as judged by the investigator
- Allergy to Streptococcus salivarius or any lozenge ingredients
- Use of other probiotics
- Use of anticoagulant medications or having blood/bleeding disorders
- Recent or upcoming dental, oral, or other surgeries
- Use of anti-plaque or anti-gingivitis products
- Active infections
- Experiencing nausea, fever, vomiting, bloody diarrhea, or severe abdominal pain
- Use of any antibiotics
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Toronto
Toronto, Ontario, Canada, M5G 1G5
Actively Recruiting
Research Team
M
Mark Kwiecinski, P.Eng, M.Sc Physics
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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