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Functional Appliance for Orthognathic Surgery

Post-surgical Stability in Mandibular Advancement Using Postsurgical Versus Presurgical Computer Guided Functional Appliance. (RANDOMIZED CLINICAL TRIAL)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05009056
Enrollment
18
Registered
2021-08-17
Start date
2021-06-01
Completion date
2024-05-01
Last updated
2024-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthognathic Surgery

Brief summary

The unstable condylar position in the glenoid fossa is a critical problem for postsurgical instability after mandibular advancement with subsequent mandibular relapse. The habitual forward occlusion in class II patients creates unstable condyle to glenoid fossa relationship making it hard for clinicians to determine the amount of mandibular advancement. Splint therapy is considered as a preoperative reversible nonsurgical condylar repositioning option in addition to its adjunctive effect for pain relief in TMJ symptomatic patients. To minimize this relapse, presurgical functional appliance therapy has been proposed and has shown promising outcomes.

Detailed description

The aim of this study is to compare the effect of postsurgical versus presurgical computer guided functional appliance in relapse prevention after mandibular advancement surgery. Surgical procedure: 1. Owbgeser incision will be performed to expose the buccal and lingual aspects of the ramus angle region. 2. CAD/CAM generated preoperative wafer will be placed on the lower arch dentition, the guide has an extension to guide medial, vertical, oblique cuts as well as screw holes for reference landmarks for proximal segment & tooth bearing segment. 3. Drilling of all the reference landmarks on the proximal segment and locating medial, vertical, oblique cuts. 4. Removal of guide, then BSSO is performed. 5. The final wafer is placed, the guiding hole on the proximal segment will then be realigned with the previously drilled screw holes, fixation using mono cortical screws then drilling screw holes for plate fixation. 6. Fixation of the osteotomy using 2.0 mm pre-bent mini plates. 7. A positioning screw will be added to improve stability against rotational forces. b-Functional appliance Postsurgical computer guided functional appliance: After achieving ideal condylar poison by computer guided surgery. The distal extension of the final occlusal wafer will be cut and the appliance will be fitted to be utilized as a postsurgical functional appliance for condylar adaptation. Patients will be instructed to wear the splints continuously for 3 months, only being allowed to remove them when eating and brushing their teeth. Presurgical computer guided functional appliance: Using the software, 3D digitized mandible will be virtually repositioned in ideal centric relation through accurate adjustment of the condyle in its glenoid fossa. Patients' dental casts will be scanned, and digitized into a virtual 3D model and superimposed to the CT cuts into the virtual plan software environment in order to produce preoperative CAD/CAM splint on the adjusted centric occlusion. Patients will be instructed to wear the splints continuously for 3 months, only being allowed to remove them when eating and brushing their teeth. c- Follow up All patients will be advised to stay on a soft diet for 4-6 weeks to avoid any undue forces on the surgical site. Postoperative CT and lateral cephalogram will be obtained, immediately postoperative and 12 months later respectively.

Interventions

DEVICEPostsurgical computer guided functional appliance

After achieving ideal condylar poison by computer guided surgery. The distal extension of the final occlusal wafer will be cut and the appliance will be fitted to be utilized as a postsurgical functional appliance for condylar adaptation. Patients will be instructed to wear the splints continuously for 3 months, only being allowed to remove them when eating and brushing their teeth.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Single blinding

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Age of the patient above 18 years * Patients in need of bilateral sagittal split osteotomy for mandibular advancement. * All patients are free from any systemic disease that may affect normal bone healing. * Sufficient dentition to reproduce the occlusal relationships * Patient's consent to participate

Exclusion criteria

* Patients with any systemic disease that may affect normal healing * Intra-bony lesions or infections that may interfere with surgery * Previous orthognathic surgeries

Design outcomes

Primary

MeasureTime frameDescription
Change from postoperative sagital position of the mandible at 12 months (skeletal stability)immediately postoperative and 12 months laterMethod of Measurement: Lateral cephalogram Unit of Measurement: mm

Secondary

MeasureTime frameDescription
Assessment of condylar deviationimmediately postoperative and 12 months laterMethod of Measurement: CT scan Unit of Measurement: mm

Other

MeasureTime frameDescription
Distal segment linear deviationimmediately postoperative and 12 months laterMethod of Measurement: CT scan Unit of Measurement: mm
Distal segment angular deviationsimmediately postoperative and 12 months laterMethod of Measurement: CT scan Unit of Measurement: degree

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026