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).
Eligibility criteria
Qualifiers
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.
Disqualifiers
Planning a move within 9 months.
Unwilling to provide two phone numbers and two email contacts.
Not willing to express a willingness to come in for 4-6 month follow up if they have marked improvement or improvement in symptoms.
Not living within 90-minute drive from clinic
Trial design
Treatments tested in this trial
- 3D Analysis Group
- Manual Analysis Cohort
Treatment groups
Sponsors and collaborators
Dr. Dean Reeves Clinic
Lead sponsor
Lourens A. Du Preez
Collaborator