Effect of Phototherapy in Individuals With Temporomandibular Disorder.

Phase 2UnknownNCT02018770

University of Nove de Julho48 enrolled

Overview

The present study aims to evaluate the effect of phototherapy with the combination of different sources of light on pain, activity of temporal and masseter muscles, bilateral and joint mobility in subjects with TMD. It will be made a randomized, placebo-controlled and double-blind clinical trial. Individuals participate with myogenic temporomandibular disorder, being allocated into 4 groups randomly and stratified by the method of sealed envelopes. The results will be evaluated using: RDC/TMD, digital caliper, electromyography, and visual analog scale and algometry. The protocols will be used in a single session and will be evaluated in four different moments. The variables that will be investigated are pain, muscle activity and joint mobility. The analyses of the data will be performed by adopting a significance level of 5%.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Temporomandibular Disorder.

Interventions

Portable Cluster 9 PainAway ® diodes manufactured by Multi Radiance Medical ® (Solon, OH-USA), being 1 905 nm diode (1 mW average power 10 W of peak power, spot of 0.44 cm2), 875 nm diodes 4 (17.5 mW average power for each diode, spot of 1 cm2) and 670 nm diodes 4 (15 mW average power for each diode1 spot, cm2), frequency of 1000 Hz, irradiation time of 300 seconds, energy delivered from 39.3 Joules.

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 40 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 18 to 40 years. * Female volunteers. * Diagnosis of myogenic TMD pain must masseter presenting moderate to severe according to the RDC / TMD. * Display body mass index (BMI) less than 25 kg/m2 to standardize the sample. * In addition, volunteers must submit scores of pain greater than 3 cm according to the Visual Analog Scale masticatory muscles. Exclusion Criteria: * history of neurological disorders. * chronic neck pain resulting from a traumatic incident. * chronic musculoskeletal condition. * medical diagnosis of fibromyalgia; systemic disease. * connective tissue disorder. * having undergone physical therapy use of analgesic, muscle relaxant.

Outcomes

Primary Outcomes

Pain intensity.

Will be used a algometry D-200 of Instrutherm ®, which is a semi quantitative method to measure the intensity of the pain by the pressure, find painful spots, in addition to quantify changes the various pain syndromes.

Time frame: 1 year

Secondary Outcomes

Electromyographic activity

The electrical powers of masticatory muscles will be verified in this study through surface electromyography, specifically the masseter and temporal muscles, serving as a useful tool to quantify muscle activity during Mastication and thus identify its functional changes.