Prospective Registry of 3-dimensional Virtual Treatment Planning of Orthognathic Surgery
Sponsored by AZ Sint-Jan AV
About this trial
Last updated 4 years ago
Study ID
Status
Type
Placebo
Accepting
Not accepting
Trial Timing
Started 15 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
- Patients of all ages
- Both female and male patients
- Patients should present themselves at the Department of Oral and Maxillofacial Surgery of the General Hospital Saint-John Bruges for orthognathic surgical treatment
- Patients receive standardized cone-beam computed tomography (CBCT) image acquisition (i-CAT, Imaging sciences international, inc, Hatfield, USA) according to the "triple" CBCT scan protocol
- Patients' orthognathic surgery should be prepared by a standardized setup of an augmented 3D virtual patient model in centric relation, with detailed occlusal and intercuspidation data using the "triple" voxel-based rigid registration protocol (Maxilim v2.2.2., Nobel Biocare c/o Medicim nv, Mechelen, Belgium)
- Patients' surgery should be prepared preoperatively through 3D virtual planning steps performed with the same software, by the same surgeon (GS)
- Patients should be operated by the same surgeon (GS)
Exclusion Criteria
- All patients that do not fit in the abovementioned description
- Patients with posttraumatic deformity
- Patients with congenital deformity
- Patients with preprosthetic indication