None listed
Conditions
Brief summary
The main purpose of this controlled clinical trial is to investigate the efficcacy of low level laser therapy in the treatment of Burning Mouth Syndrome patients, considering the mucosa affected and level of discomfort. Evaluation will be performed through visual analogue scales and a global perceived effect questionnaire after four laser irradiations sessions and a ninety days follow-up period.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
Patients with burning mouth syndrome presenting symptoms at least for 6 months.
Exclusion criteria
Patients with lesions on the oral mucosa that may be related to the burning sensation