Temporomandibular Joint Syndrome
Conditions
Interventions
A randomized, controlled, double-blind, longitudinal clinical trial. In the first stage, 84 participants will be selected and divided into three groups of 28 each, where one will have as an interventi
E02.760.169.063.500.387
Sponsors
Universidade Federal de Sergipe
Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará
Eligibility
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Individuals of both sexes; aged between 18 and 70 years; with at least 20 natural dental elements (10 on each side); diagnosed with muscular type temporomandibular disorders (TMD)
Exclusion criteria
Exclusion criteria: Individuals with any inability to answer questions asked during care; patients who are already using therapeutic ultrasound or another type of therapy for muscle fatigue
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in chewing performance by scanning mascara gum for chewing cycles. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to verify an improvement in pain using an algometer and EVA scale, in muscle activity through electromyography, in bite force through a dynamometer, in quality of life through the SF-26 and possible adverse effects through the Naranjo algorithm. | — |
Countries
Brazil
Contacts
Public ContactPatricia Serpa
Universidade Federal do Ceará
Outcome results
None listed