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Clinical Trials/NCT02294799
NCT02294799
Not yet recruiting
Not Applicable

Magnetic Ressonance Imaging Evaluation of Articular Disc Position in TMD Subjects After Mandibular Mobilization. A Double Blind, Randomized, Placebo-controlled Study

Daniela Ap. Biasotto-Gonzalez1 site in 1 country24 target enrollmentAugust 2026

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Temporomandibular Joint Dysfunction
Sponsor
Daniela Ap. Biasotto-Gonzalez
Enrollment
24
Locations
1
Primary Endpoint
Articular Disc Positioning (Measured by the Magnetic Ressonance Imaging)
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Background: Among the instrumental devices that have been proposed over the years to integrate the clinical evaluation of temporomandibular joint disorders (TMD), imaging techniques are the most studied, showing that magnetic resonance imaging (MRI) is the technique most need to describe the anatomy of the TMJ and to evaluate the correlation of imaging findings with the clinical diagnosis . Despite the amount available studies on the use of MRI for evaluation of TMJ disorders and treatments, there is a lack of studies that evaluate the imaging findings after physical therapy. Purpose: To evaluate the influence of nonspecific mandibular mobilization about the positioning of the articular disc by MRI in individuals with TMD diagnosis of anterior disc displacement with and without reduction according to the Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD). Analyze the behavior of pain through the numerical scale of pain assessment (END) at baseline and after each treatment session, the quality of life of individuals with TMD at baseline, immediately, three and six months after the treatment sessions by the World Health Organization Quality of Life Assessment (WHOQOL - BREF), and The Patient's Specific Functional Scale (PSFS) at baseline and after treatment. The treatment will be performed three times a week during four weeks. Metodology: This is a randomized, placebo controlled, blind study designed to assess the effects of techniques nonspecific mandibular mobilization x placebo. Individuals will be randomized and divided into two groups: Group A (intervention) and Group B (placebo). Statistic analysis: The positioning of the articular disc, extracted through the use of MRI, will be considered the primary outcome and, as a secondary outcome will be assessed the quality of life, pain and function after treatment. The adherence of the data to a Gaussian curve will be verified by the Shapiro-Wilk and the data are expressed as mean values and standard deviation. Two-way repeated measures analysis of variance with Bonferroni post hoc test will be used for inter-and intra-group comparisons. The significance level is adjusted p ≤ 0.05.

Detailed Description

This is a randomized, placebo-controlled, double-blind study designed to verify the effects of nonspecific mandibular mobilization techniques x placebo

Registry
clinicaltrials.gov
Start Date
August 2026
End Date
December 2028
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Daniela Ap. Biasotto-Gonzalez
Responsible Party
Sponsor Investigator
Principal Investigator

Daniela Ap. Biasotto-Gonzalez

Phd

University of Nove de Julho

Eligibility Criteria

Inclusion Criteria

  • TMD diagnosed subjects by RDC / TMD confirmed by the MRI findings,
  • with anterior disk displacement with or without reduction,
  • with full dentition (excluding third molars).

Exclusion Criteria

  • Subjects diagnosed TMD exclusively muscular;
  • with posterior and / or medial displacement of the disc;
  • showing systemic diseases that affect the joints and / or masticatory muscles;
  • neuromuscular diseases;
  • hypo / condylar hyperplasia;
  • making use of any type of dental prosthesis;
  • are in orthodontic and / or physical therapy;
  • showing neurological or behavioral disorders that preclude the achievement of MRI and/or
  • a history of previous TMJ surgery.

Outcomes

Primary Outcomes

Articular Disc Positioning (Measured by the Magnetic Ressonance Imaging)

Time Frame: Baseline (day 1) and after 4 weeks of treatment performed 3 times a week.

Measured by the Magnetic Ressonance Imaging

Secondary Outcomes

  • Clinical Symptoms (Measured by END)(Baseline (day 1) and after 4 weeks of treatment performed 3 times a week.)
  • Functionality (Mesuread by "The Patient´s Specific Funcional Scale - HORN, 2012)(Baseline (day 1) and after 4 weeks of treatment performed 3 times a week.)
  • Quality of life (Whoqol-bref)(Baseline (day 1) and after 4 weeks of treatment (performed 3 times a week), 3 and 6 months follow up)

Study Sites (1)

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