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Study of Temporomandibular Joint Dysfunction

Study of Movement of the Pathological Temporomandibular Joint.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03305315
Acronym
CinématiqueATM
Enrollment
15
Registered
2017-10-09
Start date
2017-12-12
Completion date
2019-11-22
Last updated
2021-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diseases of the Temporomandibular Joint

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.

Interventions

OTHERMeasurements of jaw movement

Jaw mobility will be measured during simple movements of the mouth (opening the mouth, side-to-side and backwards-and-forwards movement of the jaw). These movements will be measured using a specific apparatus, part of which will be placed on the head like a helmet with the other part placed in the mouth and stuck to the teeth using a dental adhesive. The part in the mouth is specifically designed for this purpose. Measurements using this apparatus will take around 30 minutes.

OTHERMeasurement of natural electrical activity of facial muscles

Natural electrical activity of the facial muscles will be measured using electrodes placed on the skin.

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patients: * 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, * Absence of clicking, popping, or grating sounds during large movements and during palpation of the TMJ with the mouth slightly open (distance between incisors around 1 cm) * Absence of headache, * Absence of tinnitus, * Kinematic curves around the mean.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Mobility of the jaw with regard to the skull during each movement.Until 6 months post-surgery

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026