A Multicenter RCT to Investigate the Treatment of Double (Bilateral) Mandibular Fractures



Status:Active, not recruiting
Conditions:Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:1/20/2019
Start Date:April 2015
End Date:May 2019

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A Multicenter Randomized Controlled Clinical Investigation to Investigate the Treatment of Double (Bilateral) Mandibular Fractures

Mandibular fractures represent approximately 50% of the total facial fractures and are
commonly (more than half) presented in more than one location. A few simple fractures can be
treated using a conservative approach. More often, however, mandibular fractures require
stabilization using open reduction and internal fixation.

Simple mandibular fractures can be treated using non-rigid fixation techniques that rely on
the load-sharing principle, by which stabilization is accomplished with both fixation devices
and bone surfaces. On the other hand, more complex fractures with continuity defects or
comminuted need to be handle using rigid fixation where the device assumes all the forces
(load-bearing principle). These approaches are well established, whereas the level of
evidence for the treatment of bilateral double mandibular fractures (DMF) is still scarce. In
fact, which surgical treatment, or combination of treatments, leads to the best outcome and
the lowest rate of complications in bilateral DMFs is an open question.

The purpose of this study is to assess the complication rate in patients suffering from
bilateral DMF treated either using non-rigid fixation on both fracture sides or a combination
of rigid fixation on one side and non-rigid fixation on the other side.

Prospective data will be collected in 314 patients suffering from bilateral (double)
mandibular fracture randomly treated either with non-rigid fixation on both fracture sides or
a combination of rigid fixation on one side and non-rigid fixation on the other side. This is
a study where patients will be treated per randomization to one of the two established
treatments and followed for further clinical examination post-operatively at 6 weeks and 3
months after the intervention.

Inclusion Criteria:

- Age 18 years or older at the date of the surgery

- Diagnosis of bilateral (double) mandibular fracture located in:

- Angle and body or

- Angle and symphysis or

- Body and symphysis

- Dentition: Patients must have most of their maxillary and mandibular teeth present and
it must be possible to identify proper occlusion. The application of intraoperative
Mandibulo-maxillary fixation (MMF) using arch bars must be possible

- Ability to understand the content of the patient information / Informed Consent Form

- Willingness and ability to participate in the clinical investigation according to the
Clinical Investigation Plan (CIP)

- Signed and dated IRB/EC-approved written informed consent

Exclusion Criteria:

- Fractures displaying continuity defect or comminution

- Fractures showing clinical signs of infection at presentation

- Edentulous mandible fracture

- Fractures requiring an extra-oral surgical approach

- Concomitant maxillary fractures

- Concomitant condylar fracture

- Prior surgical treatment of the mandibular fracture(s)

- Atrophy of the mandible (<20 mm vertical height) at the level of the fracture(s)

- Polytrauma (i.e. severe injuries leading to life-threatening condition)

- Prisoners

- Participation in any other medical device or medicinal product study within the
previous month that could influence the results of the present study
We found this trial at
5
sites
201 Presidents Circle
Salt Lake City, Utah 84108
801) 581-7200
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