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Orthognathic Surgery With Clear Aligners vs Conventional Brackets

Perioperative Outcomes in Orthognathic Surgery With Clear Aligners Versus Conventional Brackets: A Retrospective Comparative Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07511296
Enrollment
420
Registered
2026-04-06
Start date
2020-01-01
Completion date
2025-09-03
Last updated
2026-04-06

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

Conditions

Dental Deformity, Malocclusion, Orthognathic Surgery

Brief summary

This retrospective single-center observational study compared perioperative and early postoperative outcomes in patients undergoing orthognathic surgery after orthodontic preparation with either conventional fixed brackets or clear aligners. The objective was to assess whether aligner-based preparation was associated with differences in intraoperative occlusal management, including fixation stability, technical difficulties, need for additional intraoperative adaptations, and early occlusal outcomes.

Interventions

DEVICEConventional fixed orthodontic appliances

Orthodontic preparation with fixed multi-bracket appliances in place at the time of surgery, providing conventional anchorage for intermaxillary fixation and intraoperative occlusal control.

Orthodontic preparation with clear aligners and no fixed brackets at the time of surgery. Alternative intraoperative strategies may be required to achieve planned occlusal positioning and stabilization.

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing orthognathic surgery at the study center during the study period. * Orthodontic preparation with either conventional fixed brackets or clear aligners. * Age 16 years or older. * Available perioperative clinical records and required imaging data.

Exclusion criteria

* Missing perioperative data required for the analysis. * Missing preoperative or postoperative imaging required for assessment. * Explicit opposition to the reuse of data, if applicable. * Syndromic conditions. * Cleft-related deformities. * Distraction osteogenesis. * Secondary surgery. * Follow-up \< 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Composite perioperative occlusal management eventFrom surgery to the immediate postoperative assessmentNumber of composite perioperative occlusal management event for each patient

Secondary

MeasureTime frameDescription
Stable intermaxillary fixationFrom begining to the end of the surgeryNumber of stable intermaxilary fixation or not for each patient
Surgical revision after surgeryAfter surgery and the next 6 monthsNumber of patient with postoperative complications 6 months after surgery

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 7, 2026