Inclusion Criteria |
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* 18 years of age and older |
* at least 20 intact natural teeth |
* 2 or more lesions, one of which being a cavitated D2 or D3 |
* willing and able to provide informed consent |
Exclusion Criteria |
* pregnant or planning to become pregnant during the study (breastfeeding is permitted) |
* use of fixed orthodontic appliances |
* allergic to any of the ingredients of the study medication (chlorhexidine diacetate, Sumatra benzoin, alcohol, ammonio methacrylate copolymer type B, or triethyl citrate) |
* long-term antibiotic therapy (defined as taking an antibiotic -- including low dose doxycycline (Periostat) - for 30 days or more in the past 3 months) |
* currently taking any anti-fungal medication prescribed by a doctor or dentist |
* a history of, or currently active, radiation therapy for cancers of the head or neck |
* Sjögren's syndrome |
* advanced periodontitis and in the clinical judgment of the examiner, there is the likelihood the participant will not have 20 natural teeth at the end of the study |
* having ten or more teeth requiring restorative care at the time of the screening visit |
* requires antibiotic prophylaxis for dental care |
* remineralization therapy within one month of randomization (includes use of a fluoride varnish, 5000 ppm prescription fluoride toothpaste, a 0.12% chlorhexidine mouth rinse or gel, sodium fluoride mouth rinse, use of Xylitol products, by mouth, two or more times per day for four or more days per week (excluding Trident) |
* investigator discretion |