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New tooth test could spot hidden jaw problems

NCT ID NCT07185711

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 2 times

Summary

This study checked how stable teeth are in people with cemento-osseous dysplasia (COD), a rare jaw condition that can affect tooth attachment. Researchers used two non-invasive tools—a device that measures tooth vibration and a bite force sensor—to compare affected teeth with healthy ones in 17 patients. The goal was to see if these simple tests could detect changes in tooth stability caused by COD, which might help doctors diagnose and monitor the condition without X-rays or surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to better, non-invasive ways to assess tooth stability in people with cemento-osseous dysplasia, helping dentists monitor the condition more accurately.
What could go wrong
This was a very small study (17 people) and only measured immediate stability. It does not test any treatment or long-term outcomes, so the findings may not apply to all patients or predict future tooth problems.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

17 people

The number who actually took part.

Started

Jan 2025

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients diagnosed with cemento-osseous dysplasia (COD) based on panoramic radiographs * Presence of at least one COD-associated tooth suitable for measurement * Availability of a contralateral healthy tooth to serve as a control * Teeth with healthy periodontal supporting tissues * Patients aged ≥18 years * Patients who have provided written informed consent Exclusion Criteria: * Presence of systemic diseases that could affect bone or periodontal structures (e.g., uncontrolled diabetes, osteoporosis, metabolic bone diseases) * History of radiotherapy or chemotherapy in the head and neck region * Teeth with extensive caries, mobility, or periodontal disease * Patients with a history of orthodontic treatment or trauma in the relevant region

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Eskişehir Osmangazi University

    Eskişehir, 26480, Turkey (Türkiye)