Laser or pill? new study tests two treatments for chronic mouth pain
NCT ID NCT07381361
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests two treatments for burning mouth syndrome, a condition causing ongoing mouth pain without visible cause. One treatment uses low-level laser therapy (light energy), and the other uses a supplement called alpha-lipoic acid. Sixty adults with the condition will receive one of the two treatments for two weeks, and their pain levels will be measured using a standard pain scale.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- low-level laser therapy and alpha-lipoic acid
- What this could lead to
- If successful, this could point toward a non-drug, low-risk option for managing chronic burning mouth pain.
- What could go wrong
- This is a small, early-stage trial with only 60 participants. The treatments may not prove more effective than placebo, and results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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Apr 2025
- Expected to finish
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Mar 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 to 75 years * Diagnosis of Burning Mouth Syndrome (BMS) according to the 3rd edition of the International Classification of Headache Disorders (ICHD-3) * Daily intraoral burning or dysesthesia lasting for more than 2 hours for over 3 months * Normal oral mucosa and sensory testing * Condition not better accounted for by another ICHD-3 diagnosis Exclusion Criteria: * Other oral mucosal diseases, such as oral leukoplakia or oral lichen planus * Diabetes with poor blood glucose control * Hematological diseases * Pregnancy or lactation * Severe mental disorders preventing cooperation with treatment * Heart failure (New York Heart Association class III-IV)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
West China Hospital of Stomatology, Sichuan University
Chengdu, Sichuan, 610041, China
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Other studies related to the condition(s) this trial covers.
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