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New MRI study aims to better understand jaw joint disease
NCT ID NCT07008690
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses MRI scans to track changes in the jaw joint over 18 months in people with degenerative joint disease. Researchers will compare these scans to those from healthy volunteers to learn more about how the disease progresses. No drugs or contrast agents are used. The goal is to gather information that could help design future studies.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Participants with DJD will be recruited during routine examinations at the TMD clinic located at the School of Dentistry, UMN. If eligible and interested, participants will undergo approximately 90 minutes of qMRI scans. Additional follow-up scans may occur over 18 months, while control participants will have two scans 1-4 weeks apart.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: 1. To participate in this study, patients (with DJD) must: * Be 18 years or older * Provide written informed consent in English * State willingness to comply with all study procedures and be available for the duration of the study * Have clinically confirmed DJD diagnoses based on CT and/or radiographs, and /or traditional MRI scan obtained by their clinician. * Willing to have a separate approximately 2-hour appointment to have an MRI at the CMRR * Has the ability to manage their own calendar and schedule appointments * Does not have a serious medical condition * Is not pregnant or is not potentially pregnant 2. To participate in this study, controls (participants without DJD) must: * Be 18 years or older * Provide written informed consent in English * State willingness to comply with all study procedures and be available for the duration of the study * Confirm the absence of any pre-existing TMJ disease * Willing to have a separate approximately 2-hour appointment to have an MRI at the CMRR * Has the ability to manage their own calendar and schedule appointments * Does not have a serious medical condition * Is not pregnant or is not potentially pregnant 3. Exclusion Criteria: Participants will be excluded if they: * Contraindications to MRI. Exclusion criteria for MRI are: 1. Ferromagnetic implants 2. History of shrapnel or shot gun injury 3. Too large to fit in the magnet (body mass index \>= 40, approx.) 4. Cardiac pacemakers 5. Severe claustrophobia 6. Large tattoos 7. History of metalwork * Are non-English speaking * Could be pregnant
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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
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Orofacial MRI Center at UMN
Minneapolis, Minnesota, 55455, United States
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