Burning Mouth Syndrome Clinical Trial
Official title:
Study Evaluating the Laser Diode Effect on Burning Mouth Syndrome
The aim of this study was to report the effect of laser diode on the treatment of burning
mouth syndrome (BMS)
Patients were randomly allocated to two different groups:
the first one (group A) underwent Laser diode whereas the second one (group B) received
Laser diode inactive
The inclusion criteria were as follows: (a) oral burning sensation, at least in the last 6 months; (b) no detection of oral mucosal lesions; and (c) ability to complete the present clinical trial. The exclusion criteria were as follows: (a) diagnosis of Sjögren syndrome on the basis of European criteria ; (b) previous head and neck radiotherapy; (c) diagnosed lymphoma; (d) hepatitis C infection; (c) pregnant or breast-feeding women ;
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