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Temporomandibular Joint DisordersEMDJWNCT05710952

Impact of Orthodontic Treatment on the Temporomandibular Joints (TMJ) Assessed by Modjaw

A study testing Review by Modjaw in people with Temporomandibular Joint Disorders, run by University Hospital, Montpellier at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of the study is to assess the correlation between orthodontic treatment and temporomandibular joint (TMJ). For that, an evaluation with a virtual articulator (Modjaw) is carried out before and after the treatment. The condylar course are compared. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Temporomandibular Joint Disorders
What is being tested?
Review by Modjaw
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
1 siteFrance
Study dates
7 Feb 2023to 28 Sep 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Major patient (≥18 years)
  • First dentofacial orthopedic consultation at the dental clinic of Montpellier
  • Patient requiring multi-attachment orthodontic treatment (vestibular or lingual) for a duration ≤2 years
  • Signed informed consent

Who cannot join

  • Syndromic patient
  • Orthodontic treatment with aligners
  • General joint or bone pathology
  • Patients with oral hygiene incompatible with orthodontic treatment

Trial locations and contacts

1 site in 1 country.

France1 site
  • Centre de soins dentaires

    Montpellier, 34000

Other trials in France

About this study

Official title: Impact of Orthodontic Treatment on the Temporomandibular Joints (TMJ) Assessed by Modjaw in Adults

The aim of the study is to assess the correlation between orthodontic treatment and temporomandibular joint (TMJ). For that, an evaluation with a virtual articulator (Modjaw) is carried out before and after the treatment. The condylar course are compared. Furthermore, the eventual TMJ symptoms are also compared before and after.

Being tested
Review by Modjaw
Keywords
Temporomandibular joint, Orthodontic, Modjaw, Orthodontic braces
Medical subject headings
Temporomandibular Joint Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Review by ModjawDevice

    A review by Modjaw's will be done before the braces treatment and after.

Study groups in NCT05710952
Study groupRoleWhat they receive
BracesOtherPatients will receive an orthodontic treatment with fixed braces for 12 to 24 months
Receives: Device: Review by Modjaw

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Gap reduction between the interincisive point in mouth opening and the ordinate axis

    Define if there is an improvement in the straightness of the condylar path by measuring the gap between the interincisive point in mouth opening and the ordinate axis in mm assessed by Modjaw

    Measured: Up to 24 months

Secondary outcomes (7)
  1. Condylar courses homogeneity

    Qualitative comparison of the homogeneity of the condylar courses before and after treatment

    Measured: Up to 24 months

  2. Condylar courses symmetry

    Qualitative comparison of the symmetry of the condylar symmetry before and after treatment

    Measured: Up to 24 months

  3. Condylar courses straightness

    Qualitative comparison of the straightness of the condylar symmetry before and after treatment

    Measured: Up to 24 months

  4. Amplitude of the condylar path

    Virtual path length in mm assessed by Modjaw

    Measured: Up to 24 months

  5. Straightness of the condylar path

    Y-axis deviation in mm assessed by Modjaw

    Measured: Up to 24 months

  6. Adverses events

    Adverse events will be assessed before and after treatment

    Measured: Up to 24 months

  7. Pain assessment

    Pain is assessed by an analogic visual scale from 0 (no pain) to 10 (maximum pain)

    Measured: Up to 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Feb 2023
  2. Study start7 Feb 2023
  3. Primary completion28 Sep 2026
  4. Study completion28 Sep 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
32 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05710952
Sponsor's protocol ID
RECHMPL22_0509
Acronym
EMDJW
Status last verified
Oct 2026
First submitted
12 Jan 2023
Last updated
2 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Review by Modjaw in people with Temporomandibular Joint Disorders, run by University Hospital, Montpellier at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Gap reduction between the interincisive point in mouth opening and the ordinate axis (time frame: Up to 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Nov 2026.

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