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

C

Central Hospital, Nancy, France

Status

Not yet enrolling

Conditions

Temporomandibular Joint Disorders
Healthy

Treatments

Device: MRI with Real Time MRI Rapid Flash sequence

Study type

Interventional

Funder types

Other

Identifiers

NCT06070558
2021-A02648-33

Details and patient eligibility

About

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.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Healthy
Other group
Description:
Healthy volunteers
Treatment:
Device: MRI with Real Time MRI Rapid Flash sequence
Temporomandibular Joint Disorders
Other group
Description:
Patients with Temporomandibular Joint Disorders
Treatment:
Device: MRI with Real Time MRI Rapid Flash sequence

Trial contacts and locations

1

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Central trial contact

Pedro Augusto GONDIM TEIXEIRA, MD, PhD; Gabriela Hossu, PhD

Data sourced from clinicaltrials.gov

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