Effect of Treatments on Pain and Quality of Life in Individual With Burning Mouth Syndrome

Last updated: February 27, 2025
Sponsor: Federal University of Minas Gerais
Overall Status: Active - Recruiting

Phase

4

Condition

Hyponatremia

Skin Wounds

Oral Facial Pain

Treatment

local photobiomodulation

topical phytotherapic capsaicin gel

topical clonazepam tablet

Clinical Study ID

NCT06040190
6.161.933
  • Ages 18-70
  • All Genders

Study Summary

Burning Mouth Syndrome (BMS) is characterized by a burning sensation on the tongue or other areas of the mouth, often bilateral but occasionally unilateral. It is more prevalent in postmenopausal women. No specific ethnic or socioeconomic predisposition has been identified. The etiology and pathophysiology of BMS remain unknown. Various treatment approaches have been proposed, yielding conflicting outcomes and underscoring the need for further investigation.

Patients with BMS appear to respond well to long-term therapy involving systemic antidepressants and anxiolytics. The most promising therapeutic effects have been observed with clonazepam, which leads to a significant reduction in pain when applied topically or systemically. Capsaicin, an herbal remedy, also presents as an alternative treatment option, showing positive results in alleviating BMS symptoms when compared to a placebo. Photobiomodulation represents another non-pharmacological treatment possibility. It's analgesic action is possibly attributed to the inhibition of pain mediators. Alpha-lipoic acid (ALA) is dietary supplement employed in BMS treatment. It serves as a potent antioxidant naturally produced within the body, contributing to the mitigation of skin aging and reinforcing the effects of other biological antioxidants. Based on these findings, attempts have been made to demonstrate ALA's effectiveness in BMS management, concluding that ALA may offer benefits in this context.

Therefore, the objective of this study is to investigate, in adults with BMS, the impact of different therapeutic approaches on frequency, intensity, and location of pain, as well as on on quality of life.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • burning mouth syndrome;

  • oral pain that recurs daily for > 2 hours per day for > 3 months;

  • pain with burning quality and felt superficially in the oral mucosa;

  • oral mucosa appears normal

  • oral clinical examination, including sensory tests, is normal;

Exclusion

Exclusion Criteria:

  • pregnancy;

  • oral mucosal lesions;

  • systemic diseases such as diabetes, anemia, deficiency of vitamin B1, B2, B6, B12,Fe, Zinc, and folic acid;

  • gastroesophageal reflux;

  • previous head and neck radiotherapy;

  • Sjogren's disease;

  • allergies;

  • candidiasis;

  • unstimulated saliva flow < 0.25 ml/min and stimulated flow < 1.0 ml/min will beexcluded;

Study Design

Total Participants: 150
Treatment Group(s): 6
Primary Treatment: local photobiomodulation
Phase: 4
Study Start date:
November 01, 2023
Estimated Completion Date:
October 01, 2025

Connect with a study center

  • Federal university of minas gerais

    Belo Horizonte, Minas Gerais
    Brazil

    Active - Recruiting

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