RecruitingEarly Phase 1NCT07016555
Burning Mouth Syndrome: Symptoms and Management
Sponsor
University of Massachusetts, Amherst
Enrollment
50 participants
Start Date
Jun 11, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
This research study aims to evaluate how an oral cooling spray, currently a commercial dietary supplement, impacts symptoms associated with burning mouth syndrome (BMS). This study will examine symptoms, frequency, and severity, along with other related side effects of BMS on food intake, enjoyment, and quality of life.
Eligibility
Min Age: 18 Years
Inclusion Criteria9
- Have buring mouth syndrome or experience oral burn
- Live in the United States
- At least 18 years old
- Having been diagnosed or suspected diagnosis of burning mouth syndrome or suffer from chronic oral burn without any identifiable causative lesion
- No tongue or cheek piercings
- No history of cancer
- No recent or scheduled dental treatment
- No history of gum disease
- No aversions to mint or hop extracts
Exclusion Criteria2
- Have recently undergone dental treatment in the last three months or have plans to undergo dental treatment (e.g., fillings, crowns, root canals, extractions, or other dental procedures) in the coming month.
- Have started any new treatments for BMS in the last 3 months or have plans to start new treatments in the coming month.
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Interventions
DIETARY_SUPPLEMENTOral cooling spray
Use oral spray 3 times per day for 2 weeks
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07016555