Virtual Planning of Total Temporomandibular Joint Replacement

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorLund University Hospital

About this trial

A total TMJ replacement surgery is currently planned based on the X-ray appearance of the facial X-ray. It is now possible to use either an individually designed TMJ prosthesis or a prosthesis with a standard appearance. It is a significantly higher cost for treatment with an individually manufactured prosthesis, but it also provides the opportunity for virtual planning of the positioning of the jaws and prosthesis.

By using a planning program with treatment simulation through the use of our own virtual models for standard prostheses, virtual planning of jaw and prosthesis positioning is possible even with a standardized temporomandibular joint prosthesis. In this way, the advantages of virtual planning are partly brought to the patients at a much lower price.

This project aims to virtually plan treatment for patients with standardized temporomandibular joint prosthesis. Patients eligible for this study are included retrospectively (have already been treated). Their X-rays will be used for treatment planning and for comparison with the treatment outcome of previous TMJ treatment.

The study will analyze the possibilities of the standardized prostheses to provide the same positions, temporomandibular joint replacements and movements of the jaw as an individual temporomandibular joint prosthesis has. This is done by measuring the planned positions of standardized temporomandibular joint prostheses compared to the treatment outcome shown by previous postoperative X-ray examinations.

The study aims to clarify the possibilities of a simpler and less expensive technology, standardized temporomandibular joint prostheses, to achieve the same good treatment outcome as a more costly technology. This with the same possibilities for treatment planning and use that the existing, more expensive technology, individual temporomandibular joint prostheses, has today.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with severe pathology in the temporomandibular joint.

Previously treated with TMJ prosthesis at the department of Oral and Maxillofacial Surgery, Skåne University Hospital, Lund, Sweden.

Treatments performed during year 2010 to 2025.

Disqualifiers

None

Trial population

Patients previously treated with TMJ prosthesis at the department of Oral and Maxillofacial Surgery, Skåne University Hospital. Lund, Sweden during 2010 to 2025.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Measurements in preoperative radiographs for re-evaluation of possibilities for virtual surgical planning on standardized total TMJ reconstruction.

Measurements in images from virtual planned standardized TMJ prosthesis will include the following variables: * Maximal interface between bone tissue and prosthesis surface (mm2) * Size Fossa component * Size Mandibular component * Maximal number of fixation screws * Centre the mandibular part in the fossa part. * Angle between fossa and mandible part (frontal) * Angle between fossa and mandible part (sagittal)

Time frame
During 2026 retrospective virtual measurement on previous radiographs will be performed. Because patient treatments were performed during 2010 to 2025 the measurements will be performed 1 to 16 years after the recordings were performed

Secondary outcomes

1

Recorded surgical movements to correct a severe malocclusion.

Registrations from patient journals and radiographs will include the following variables: * Occlusal reposition * Maxillary reposition * Mandibular movement * Size Fossa component * Size Mandibular component * Use of bone transplant

Time frame
During 2026 retrospective virtual measurement on previous radiographs will be performed. Because patient treatments were performed during 2010 to 2025 the measurements will be performed 1 to 16 years after the recordings were performed.

Other outcomes

Sponsors and contacts

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Lund University Hospital

Lead sponsor

Lund University

Collaborator