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Study aim
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Effect of 940 nm LLLT on Myogenic TMD treatment
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Design
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Clinical trial with control group, parallel groups, triple blinded, randomized, phase 2 on 20 patients. The Rand function of Excel 2010 software was used for randomization.
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Settings and conduct
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20 patients with Inclusion criteria Who Refer to Urmia University Dental Public Health Ward,Enter to Study After Giving Informed Consent.For the intervention group in the light and laser clinic, 940 nm laser by Epic X biolase laser device will be used after calibration by the manufacturer,with output power of 300 mW in continuous mode, under dedicated control, With an energy density of 2.5 J / cm2 at detected sensitive points for 20 seconds, 2 times per week, totalling 4 weeks, in direct contact technique to the painful points. Control group, In the same way the laser group, will be irradiated with a placebo laser (device with laser off). Patients، Researcher and Statist are blinded of sample assignment.
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Participants/Inclusion and exclusion criteria
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Entrance criterias: limited mouth opening or function presence of pain in masticatory muscles and/or TMJs, either in clenching or in jaw movements (TMD muscular disturbance (class Ia, Ib) or arthralgia (class IIIa).
Exclusion criterias: patients who had major systemic disorders
Patients with arthralgic temporomandibular joint disorders
patients who received any form of treatment for TMD within the last month
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Intervention groups
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1.Intervention group: This group will be exposed to 940 nm laser with a power of 300 mW and to the temporomandibular joint area for 20 seconds two sessions per week for four weeks.
2.placebo group: In the same way, the placebo group will be exposed to Palsbo laser (device with laser off).
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Main outcome variables
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Patient satisfaction, Intensity of pain,The amount of mouth opening, Clicking sound, Deviation when opening the mouth.