Burning Mouth Syndrome: Symptoms and Management
Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Early Phase 1
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• 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
Locations
United States
Massachusetts
UMass Amherst
RECRUITING
Amherst
Contact Information
Primary
Alissa Nolden, PhD
anolden@umass.edu
413-577-0113
Time Frame
Start Date: 2025-06-11
Estimated Completion Date: 2025-12-15
Participants
Target number of participants: 50
Treatments
Experimental: Oral spray
Oral spray
Related Therapeutic Areas
Sponsors
Leads: University of Massachusetts, Amherst