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AzTrials

BruxismMOD-SPNCT07364552

Patient-Specific Occlusal Splints Using MODJAW Kinematics

A study testing MODJAW-Based Patient-Specific Occlusal Splint and Standard Occlusal Splint in people with Bruxism, run by Istanbul University at 1 site in Turkey (Türkiye).

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

This clinical study is designed to evaluate the effectiveness of patient-specific occlusal splints created using MODJAW, a jaw-tracking device that records 3D mandibular movements. Read more about this study

Who is it for?
Ages 18 to 50 years
Conditions the study is for
Bruxism
What is being tested?
MODJAW-Based Patient-Specific Occlusal Splint and Standard Occlusal Splint
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Oct 2025to 25 Dec 2025
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 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age 18-50 years
  • Diagnosed with mild-to-moderate bruxism or temporomandibular joint (TMJ) dysfunction
  • Willingness and ability to comply with splint use and study visits
  • Signed informed consent

Who cannot join

  • Severe dental loss or existing prosthetic devices interfering with splint placement
  • Systemic medical conditions affecting jaw function
  • History of TMJ trauma or surgery
  • Pregnancy or breastfeeding
  • Allergy to splint materials

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Istanbul university

    Istanbul, 34844

Other trials in Turkey (Türkiye)

About this study

Official title: Patient-Specific Occlusal Splints Designed Using MODJAW Kinematic Data: A Prospective Clinical Study

This clinical study is designed to evaluate the effectiveness of patient-specific occlusal splints created using MODJAW, a jaw-tracking device that records 3D mandibular movements. Occlusal splints are commonly used to treat bruxism (teeth grinding) and temporomandibular joint (TMJ) disorders, which can cause jaw pain, headaches, and worn teeth. Traditional splints are made using standard designs that do not consider each patient's unique jaw movements.

In this study, 40 participants with mild-to-moderate bruxism or TMJ dysfunction will be randomly assigned to two groups. One group will receive custom splints designed using MODJAW kinematic data, while the other group will receive standard occlusal splints. Participants will use their assigned splint for 8 weeks.

Read more

The study will measure:

Jaw movement patterns using MODJAW

TMJ pain levels

Patient comfort and satisfaction

The main goal is to determine whether MODJAW-based, patient-specific splints provide better jaw function, reduced pain, decreased teeth grinding, and higher patient satisfaction compared to standard splints.

Participants will be monitored throughout the study to ensure safety, comfort, and proper splint use. This study is expected to help dentists design more effective, personalized splints in the future and improve treatment outcomes for people with jaw disorders or bruxism.

Read the detailed description

Detailed Description:

Background and Rationale:

Bruxism and temporomandibular joint (TMJ) disorders are common conditions that can lead to jaw pain, headaches, tooth wear, and impaired quality of life. Occlusal splints are commonly prescribed to manage these conditions by stabilizing the jaw and distributing occlusal forces. Standard splints, however, are typically fabricated using uniform designs that do not account for the individual jaw movement patterns of each patient. Recent advances in digital dentistry, including the use of jaw-tracking devices such as MODJAW, allow clinicians to capture three-dimensional mandibular kinematics in real time. By using this information, occlusal splints can be designed to match the specific movement patterns of each patient, potentially improving comfort, jaw function, and clinical outcomes.

This study aims to evaluate whether patient-specific occlusal splints designed using MODJAW kinematic data provide superior clinical outcomes compared to standard occlusal splints.

Study Objectives:

To compare mandibular movement patterns between MODJAW-based patient-specific splints and standard occlusal splints.

To evaluate the effect of MODJAW-based splints on bruxism frequency and intensity.

To assess TMJ pain reduction in participants using MODJAW-based splints versus standard splints.

To determine patient satisfaction and comfort with patient-specific versus standard splints.

Study Design:

This is a prospective, randomized, controlled interventional study. Forty participants with mild-to-moderate bruxism or TMJ dysfunction will be randomly assigned to one of two groups:

MODJAW group (n=20): Participants will receive a patient-specific occlusal splint designed based on 3D mandibular kinematic data collected with MODJAW.

Standard splint group (n=20): Participants will receive a conventional occlusal splint fabricated using standard methods.

The study duration for each participant is 8 weeks, during which participants will wear their assigned splints according to instructions and attend follow-up assessments.

Inclusion Criteria:

Age 18-50 years

Diagnosed with mild-to-moderate bruxism or TMJ dysfunction

Willingness and ability to comply with splint use and study visits

Signed informed consent

Exclusion Criteria:

Severe dental loss or existing prosthetic devices interfering with splint placement

Systemic medical conditions affecting jaw function

History of TMJ trauma or surgery

Pregnancy or breastfeeding

Allergy to splint materials

Study Procedures:

Screening and Baseline Assessment:

Clinical examination of dentition and TMJ

Recording baseline jaw movements using MODJAW (for both groups)

Baseline assessment of bruxism frequency, TMJ pain (VAS score), and patient-reported comfort

Splint Fabrication:

MODJAW group: CAD/CAM splints designed using mandibular movement data captured by MODJAW

Standard group: Conventional splints fabricated according to standard occlusal design

Splint Use:

Participants instructed to wear splints nightly (or as directed) for 8 weeks

Weekly check-ins to monitor compliance and comfort

Follow-Up Assessments (Week 4 and Week 8):

Repeat MODJAW recordings to evaluate changes in mandibular movement

Assess TMJ pain, bruxism frequency and intensity

Collect patient satisfaction and comfort scores via 5-point Likert scale

Record any adverse events

Outcome Measures:

Primary Outcome: Changes in mandibular movement patterns as measured by MODJAW

Secondary Outcomes:

Reduction in TMJ pain (VAS score)

Patient-reported satisfaction and comfort

Data Analysis:

Within-group comparisons: Paired t-tests or Wilcoxon signed-rank tests

Between-group comparisons: Mann-Whitney U test

Categorical outcomes: Chi-square or Fisher's exact test

Statistical significance set at p < 0.05

Safety Considerations:

Participants monitored for adverse events related to splint use, including discomfort, tissue irritation, or allergic reactions

Participants may withdraw at any time

All data handled according to confidentiality and privacy guidelines

Significance:

This study will provide evidence on the effectiveness of patient-specific, MODJAW-guided occlusal splints in improving jaw function, reducing bruxism, and increasing patient satisfaction. The results may support the adoption of kinematic data in routine occlusal splint design and contribute to personalized dentistry approaches.

Conditions
Bruxism
Being tested
MODJAW-Based Patient-Specific Occlusal Splint, Standard Occlusal Splint
Keywords
Occlusal splint
Medical subject headings
Bruxism

What participants receive

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

  • MODJAW-Based Patient-Specific Occlusal SplintDevice

    A custom occlusal splint designed using MODJAW-recorded 3D mandibular movement data. Fabricated via CAD/CAM to fit the patient's unique jaw movements. Worn nightly (or per instructions) for 8 weeks.

  • Standard Occlusal SplintDevice

    A conventional occlusal splint made using standard methods without patient-specific mandibular movement data. Worn nightly (or per instructions) for 8 weeks.

Study groups in NCT07364552
Study groupRoleWhat they receive
MODJAW-Based Patient-Specific SplintExperimentalParticipants receive a patient-specific occlusal splint designed using MODJAW 3D mandibular kinematic data. The splint is fabricated via CAD/CAM and worn according to study instructions for 8 weeks.
Receives: Device: MODJAW-Based Patient-Specific Occlusal Splint
Standard Occlusal SplintExperimentalParticipants receive a conventional occlusal splint fabricated using standard methods. The splint is worn according to study instructions for 8 weeks.
Receives: Device: Standard Occlusal Splint

What is being measured

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

  1. Improvement in mandibular movement patterns

    Mandibular movements will be recorded using MODJAW 3D jaw-tracking system.

    Parameters include opening, lateral, and protrusive excursions, as well as path stability and range of motion.

    The primary analysis will compare baseline mandibular kinematics to post-intervention measurements between the MODJAW-based splint group and the standard splint group.

    Measured: Baseline and after 8 weeks of splint use

Secondary outcomes (2)
  1. TMJ pain levels

    Patients pain levels will be assessed using a Visual Analog Scale (VAS).

    Measured: Baseline and after 8 weeks of splint use

  2. Comfort and satisfaction

    Patient comfort and satisfaction will be assessed using a patient-reported questionnaire and 5-point Likert scale.

    Measured: Baseline and after 8 weeks of splint use

Timeline

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

  1. First posted23 Jan 2026
  2. Study start15 Oct 2025
  3. Primary completion15 Dec 2025
  4. Study completion25 Dec 2025

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants are randomly assigned to one of two groups: (1) MODJAW-based patient-specific splint group, or (2) standard occlusal splint group. Each participant follows their assigned intervention for 8 weeks. Outcomes are compared between the groups at baseline and post-intervention.
Masking
None (open label)
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07364552
Sponsor's protocol ID
U-116S697
Acronym
MOD-SP
Status last verified
Jan 2026
First submitted
12 Jan 2026
Last updated
23 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Individual participant data (IPD) from this study will not be shared. The study involves patient-specific dental records and intraoral imaging that are considered sensitive and personally identifiable. To protect participant privacy and comply with ethical standards, raw data containing personal identifiers will remain confidential and will not be made publicly available. Aggregate or de-identified summary data may be shared upon reasonable request with qualified researchers following approval from the study team and institutional review board.

Questions about this trial

What is this clinical trial studying?

A study testing MODJAW-Based Patient-Specific Occlusal Splint and Standard Occlusal Splint in people with Bruxism, run by Istanbul University at 1 site in Turkey (Türkiye).

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 5 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 23 Jan 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 Turkey (Türkiye). 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?

Improvement in mandibular movement patterns (time frame: Baseline and after 8 weeks of splint use). 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 23 Jan 2026.

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