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Recruiting Not applicable

ChAracterization of Normal and Pathological moRphological Variations of the TEMporomandibular Joint by Real-time magnetIc reSonance Imaging

NCT06070558 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-12-12
Last updated
2026-06-17

Condition(s) studied

HealthyTemporomandibular Joint Disorders

Investigational drug(s) / intervention(s)

MRI with Real Time MRI Rapid Flash sequence

MRI with Real Time MRI Rapid Flash sequence: MRI examination of temporomandibular joint with Real Time MRI Rapid Flash sequence

Study summary

The Real Time MRI Rapid Flash sequence is particularly interesting for the study of moving organs and joints.

This sequence will make it possible to characterize normal and pathological temporomandibular joint movements by MRI.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Adult: age ≥ 18 years old; * Person with the capacity to understand the instructions given; * Person affiliated to a social security scheme or beneficiary of such a scheme; * Person having received complete information on the organization of the Clinical Investigation and having signed informed consent. Exclusion Criteria: * Person with large-scale metallic dental reconstructions; * Edentulism more than 5 teeth; * Claustrophobia; * Contraindication to performing an MRI examination * Persons referred to in Articles 64, 65 and 66 of European Regulation 2017/745 on Medical Devices (RDM) and in L. 1121-5 to L1121-8 of the French Public Health Code

Primary outcome measure(s)

  • Curve representing the difference between displacement of condyles during Temporo Mandibular Joint (TMJ) movements in healthy subjects and in subjects with known Temporo Mandibular Disorder (TMD). — Baseline (day 0)

Trial sites (1)

FacilityCityRegionStatus
CHRU de Nancy Nancy France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06070558 on ClinicalTrials.gov ↗ ← All trials in France