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

NCT06619574 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2025-02-06

No results posted yet for this study

Summary

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).

Conditions

  • Temporomandibular Joint Syndrome

Interventions

DEVICE

3D Analysis Group

Dental Compass and Dental Compass software used for therapeutic splint fabrication

OTHER

Manual Analysis Cohort

Manual methods used for therapeutic splint fabrication

Sponsors & Collaborators

  • Lourens A. Du Preez

    collaborator UNKNOWN

  • Dr. Dean Reeves Clinic

    lead OTHER

Principal Investigators

  • Kenneth D Reeves, MD · K. Dean Reeves, M.D., P.A.

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-08
Primary Completion
2026-11-01
Completion
2027-03-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06619574 on ClinicalTrials.gov