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).
Standard practice in the treatment of temporomandibular dysfunction (TMD) currently involves non-radiographically-assisted manual repositioning of the jaw followed by either an in-office cone beam computerized tomography (CBCT) or tomographic X-ray of both TMJs, and further adjustment as necessary to improve the initial bite impression.\[15\] At follow up visits the therapeutic splint is modified in stages to "walk" the condyle progressively into the ideal position, such as altering side shift, lateral deviation, and rotation. During this process multiple CBCTs or tomographic X-rays, and multiple direct dentist interventions, are required to find the precise joint position, involving significant radiation exposure, and significant chair time for the dentist The key advantage of using the Dental Compass Articulator in conjunction with its software, is to identify and suggest corrections for the range of orthopedic imbalances present. Software-facilitated identification of imbalances is coupled with manipulation of yaw (anterior, posterior, lateral, or rotational movement of the mandible in a horizontal plane), pitch (rotation of the mandible in a frontal vertical plane), and roll (rotation of the mandible in a lateral vertical plane) to achieve optimal condylar and mandibular position for splint manufacture. The goals of this study are to: 1. Determine if the use of the Dental Compass Articular and its software will produce therapeutic splints for TMD accurately and successfully, and will compare favorably with a cohort treated without the Dental Compass (for number of visits, splint modifications, and required CBCTs), and 2. Confirm a clinically important reduction in airway constriction and improvement in airway volume with us of the therapeutic splint.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Dental Compass and Dental Compass software used for therapeutic splint fabrication
Manual methods used for therapeutic splint fabrication
Skalff Dental Studio and Technologies 103 C West Broadway Street #3736
Gainesville, Texas, United States
RECRUITINGNumber of clinic visits
Number of clinic visits from initial evaluation to confirmation of final therapeutic splint provision
Time frame: 3-6 months
Number of cone beam CTs (CBCTs)
Number of CBCTs obtained from initial evaluation to confirmation of final therapeutic splint provision
Time frame: 3-6 months
Number of splint modifications
Number of splint modifications obtained from initial evaluation to confirmation of final therapeutic splint provision
Time frame: 3-6 months
Gelb 4/7 position achieved during treatment (3D group only)
Yes or no for Gelb 4/7 position
Time frame: 3-6 months
Anterior joint space of 1.8 mm or more achieved during treatment (3D group only)
Yes or no for anterior joint space of 1.8 mm or more
Time frame: 3-6 months
Posterior joint space of 1.8 mm or more achieved during treatment (3D group only)
Yes or no for posterior joint space of 1.8 mm or more
Time frame: 3-6 months
Improvement in total airway volume
Change in total airway volume from use of TMJ splint
Time frame: 3-6 months
Improvement in minimum airway diameter
Change in total airway volume from use of TMJ splint
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Time frame: 3-6 months