Temporomandibular Joint (TMJ) Positioning Accuracy and Efficiency Using a Dental Compass.
Recruiting
N/A
Interventional Study
Temporomandibular Joint Syndrome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 90
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 80 (estimated)
- Sponsor
- Dr. Dean Reeves Clinic · Other
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About This Trial
This study is being performed to determine if the use of the Dental Compass Articular and its software will produce therapeutic splints for TMD accurately and successfully, compare favorably with a cohort treated without the Dental Compass (for number of visits, splint modifications, and required CBCTs).
Trial Locations
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Eligibility Criteria
Inclusion Criteria for prospective active participants:
* TMJ dysfunction and pain
* CBCT indicates a non-Gelb 4/7 position or \< 1.8 mm bone to bone interval between the mandibular condyle and mandibular fossa anteriorly or posteriorly.
Exclusion Criteria:
* Planning a move within 9 months.
* Un…
Contacts