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Transoral Versus Transbuccal Placement of Bicortical Screws During Orthognathic Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02658305
Enrollment
509
Registered
2016-01-18
Start date
2014-10-31
Completion date
2015-11-30
Last updated
2016-01-18

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

Conditions

Jaw Abnormalities, Prognathism, Retrognathia

Keywords

transoral approach, transbuccal approach, postoperative complications

Brief summary

Bicortical screws have been widely used for mandibular osteosynthesis during orthognathic surgery.Transoral placement of bicortical screws is a rigid fixation method in orthognathic surgery, which is less often used. The aim of this study was to compare postoperative outcome of transoral versus transbuccal bicortical screw placement during orthognathic surgery. This study comprises an academic, retrospective, monocentric study in which the charts of orthognathic patients operated between January 2010 and December 2012 were retrospectively reviewed. Postoperative complications were registered. Demographic, dental and surgical parameters are examined as potential risk factors for the occurence of postoperative complications.

Interventions

None listed

Sponsors

AZ Sint-Jan AV
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients of all ages * patients of all genders * patients who had undergone a bimaxillary osteotomy, a bilateral sagittal split ramus osteotomy (BSSO), a BSSO with a chin osteotomy or a trimaxillary osteotomy

Exclusion criteria

* patients where cement had been used at the osteotomy sites * patients who had undergone a multisegmented mandibular osteotomy * patients who had undergone an osteosynthesis with plates * patients where the postoperative orthopantomogram was unavailable * patients where data regarding the type of screw placement was unavailable

Design outcomes

Primary

MeasureTime frame
Postoperative complications (rate of screw removal and/or infection)within 4 weeks postoperative

Secondary

MeasureTime frame
The value of demographic, dental and surgical parameters as potential risk factors for the occurence of postoperative complicationswithin 4 weeks postoperative

Countries

Belgium

Outcome results

None listed

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