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临床试验/NCT07016555
NCT07016555招募中1 期

Burning Mouth Syndrome: Symptoms and Management

University of Massachusetts, Amherst2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年6月11日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
50
试验地点
2
主要终点
Improved symptoms

研究概览

简要总结

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.

详细描述

Why are we doing this research study?

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.

What are some of the important aspects of this research study that I should be aware of?

Timeframe: 2 weeks intervention

Use the oral cooling spray; "Dr.B's Elixir" as directed

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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.

结局指标

主要结局

Improved symptoms

时间窗: 2 weeks

Frequency, severity, and duration of oral burn between regular treatment decreases after 2 weeks of using the oral spray

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alissa Nolden

Assistant Professor

University of Massachusetts, Amherst

研究点 (2)

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