Temporomandibular Joint (TMJ) Positioning Accuracy and Efficiency Using a Dental Compass.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorDr. Dean Reeves Clinic

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

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Dr. Dean Reeves Clinic

Lead sponsor

Lourens A. Du Preez

Collaborator