Actively Recruiting

Early Phase 1
Age: 18Years +
All Genders
NCT07016555

Burning Mouth Syndrome: Symptoms and Management

Led by University of Massachusetts, Amherst · Updated on 2025-06-11

50

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Burning Mouth Syndrome: Symptoms and Management

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have burning mouth syndrome or experience oral burn
  • Live in the United States
  • At least 18 years old
  • Diagnosed or suspected diagnosis of burning mouth syndrome or 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
Not Eligible

You will not qualify if you...

  • Have had dental treatment in the last 3 months or plan to have dental treatment (e.g., fillings, crowns, root canals, extractions, or other procedures) in the next month
  • Have started new treatments for burning mouth syndrome in the last 3 months or plan to start new treatments in the next month

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UMass Amherst

Amherst, Massachusetts, United States, 01002

Actively Recruiting

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Research Team

A

Alissa Nolden, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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