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Clinical Trials/NCT03305315
NCT03305315
Completed
N/A

Study of Movement of the Pathological Temporomandibular Joint.

Centre Hospitalier Universitaire Dijon1 site in 1 country15 target enrollmentDecember 12, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diseases of the Temporomandibular Joint
Sponsor
Centre Hospitalier Universitaire Dijon
Enrollment
15
Locations
1
Primary Endpoint
Mobility of the jaw with regard to the skull during each movement.
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Given the frequency of temporomandibular joint (TMJ) dysfunction and the variations in its expression, this project intends to initiate a process of objective evaluation of mandible function and its impairment due to different diseases. The first step is to determine whether 3D kinematic quantification of the mandible would make it possible to objectively assess the effect of post-operative management on TMJ function recovery. If the first results are encouraging and show the sensitivity of the analysis of minor joint dysfunctions, the investigators will evaluate the feasibility of kinematic assessments for major TMJ dysfunctions and for the follow-up of patients.

The expected benefits of this study are to be considered in the medium term and concern the possibilities offered by measuring mandible kinetics in the treatment of TMJ disorders.

Registry
clinicaltrials.gov
Start Date
December 12, 2017
End Date
November 22, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients who have provided verbal consent,
  • Patients over 18 years old,
  • Patients with mandible dentition compatible with placement of the kinetic measurement device,
  • Patients with a TMJ disease requiring surgery (irreducible dislocation of the joint disc, damage to the joint disc requiring discectomy, ankylosis or severe arthritis of the mandible requiring mandible implants or a TMJ prosthesis).
  • Asymptomatic subjects:
  • Subjects who have provided verbal consent,
  • Subjects over 18 years old,
  • Subjects with Class 1 occlusion,
  • Subjects without dental implants,
  • Subjects with no history of joint dysfunction,

Exclusion Criteria

  • Adults under guardianship,
  • Patients without national health insurance cover.

Outcomes

Primary Outcomes

Mobility of the jaw with regard to the skull during each movement.

Time Frame: Until 6 months post-surgery

Study Sites (1)

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