- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06838377
Accuracy of Computer Guided Screw Holes Locating Guide and Patient Specific Champy Plate vs Conventional Champy Plate Osteosynthesis in Management of Mandibular Angle Fracture: Randomized Controlled Trial
Study Overview
Status
Conditions
Detailed Description
This study will be conducted on 10 patients For each group selected from the Outpatient Clinic of the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Cairo University. Patients included in the study will have mandibular angle fracture indicated for open reduction and internal fixation. Patients with any systemic disease that could affect bone healing will be excluded from the study.
After accepting to be enrolled in this study, all patients will be subjected to:
I. Preoperative Assessment:
A thorough preoperative assessment of all patients will be carried out, including:
1. Dental and Medical history:
- Age
- Gender
- Health status 2. Clinical examination:
- Check vital signs (blood pressure, pulse, temperature, breathing).
- Examining soft tissue lacerations, paresthesia, swelling, hematoma. 3. Imaging:
- All patients will have DICOM CT scans with a slice thickness of 0.3-0.5 mm and covering a comprehensive field of view, encompassing the whole facial bones till the hyoid bone.
- Either silicon impressions or digital 3d scan via intraoral scanner to upper and lower dental arches are achieved.
These scans will be used to:
- Diagnosis purposes: assessment of fracture: location, displaced or non-displaced, favorable or non-favorable, simple or compound or communited.
- Digitally segment and realign the fracture segments.
II. Digital planning and custom made Champy plate manufacturing:
Dental arches will be segmented and waxed to the ideal occlusal relationship either by mounting on semi adjustable articular or digitally. Superimposed on the CT scan using specialized software, (3Matic software Mimics-Materialize, Belgium) which also segment and realign the fracture segments virtually.
Biomedical engineers will design the custom made Champy plate adapted on the ventral surface of the exterior oblique ridge (Champy's line of osteosynthesis) ensuring there is adequate clearance of the screw hole positions and screw lengths on the plate to avoid critical nerves, blood vessels, and adjacent teeth.
Biomedical engineers will also design a screw hole locating device 3D printed of resin.
The provisional plate design will then be forwarded to the Oral and Maxillofacial Surgeon for their final approval before the digital files of the plate is sent for manufacturing.
The custom made Champy plate will be 3D printed in titanium using laser sintering of titanium powder (Cerea and Dolcini, 2018) with heat treatment post-processing.
III. Surgical procedures the operation will under general anesthesia with nasal intubation and oral pack, Injection of 20 cc saline adrenaline 1:00000 to 0 in the sulcus for hemostasis, Vestibular mucosal incision, Reflect the flap to visualize the broken segments.
Full thickness mucoperiosteal flaps were then carefully raised to expose enough underlying alveolar bone to accommodate the screw holes locating guide and the custom-made Champy plate.
In Group I, Put the specific screw holes locating device in place and drill the screw holes, remove the screw holes locating device and mobilize the segments then apply the custom-made Champy plate and fix it with screw for passive reduction of the segments. Then suture the mucosa.
In Group II, mobilize the broken segment first, Arch bar was made to achieve proper occlusion put the Champy 2.0 plate on the ventral surface of the external oblique of the mandible and remove it for further bending using plate pliers for further accommodation of the plate then fix it in place using mono cortical screws.
IV. Evaluation protocol Scheduled follow-up intervals were 1, 2, 4, 8 and 12 weeks postoperatively. Postoperative complications, defined as a need for further intervention, were detailed prospectively over a period of at least 6 months postoperative.
Radiographic assessment will be achieved by CT scan preoperatively and postoperatively within one week to assess the following:
- to calculate any amount for segments deviation from the virtual plan in mms.
- For prevention of complications: hematoma, swelling, dehiscence and infection.
V. Statistical Methods:
- Descriptive statistics, including means and standard deviations, will be calculated to summarize the data. The statistical analysis will be performed using SPSS statistical software version 22 (IBM, Armonk, NY). The analysis will be conducted by a single statistician from Cairo University, cairo, Egypt.
- For the evaluation of primary and secondary outcomes, the chi-square statistic will be used. A significance level (p-value) of less than 0.05 will be considered statistically significant, indicating a significant difference between groups or variables.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt, 11511
- Cairo University
-
Contact:
- ahmed abdellatif, bachelor
- Phone Number: 00201119720141
- Email: ahmed.tageldeen12345@gmail.com
-
Contact:
- ahmed abdellatif, bachelor
- Phone Number: 0020115730795
- Email: ahmed.tageldeen@dentistry.cu.edu.eg
-
Cairo, Egypt, 3753450
- Cairo University
-
Contact:
- ahmed abdellatif, bachelor
- Phone Number: 00201119720141
- Email: ahmed.tageldeen12345@gmail.com
-
Contact:
- ahmed abdellatif, bachelor
- Phone Number: 00201115730795
- Email: ahmed.tageldeen@demtistry.cu.edu.eg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients with isolated mandibular angle fracture needs open reduction and internal fixation.
- Patients with medical history that did not hinder plate placement and adequate proper oral hygiene.
- Both genders males and females will be included.
Exclusion Criteria:
- General contraindications to surgery. .
- Patients with comminuted fractures.
- Subjected to irradiation in the head and neck area less than 1 year before fixation.
- Untreated periodontitis.
- Poor oral hygiene and motivation.
- Uncontrolled diabetes.
- Pregnant or nursing.
- Substance abuse.
- Psychiatric problems or unrealistic expectations.
- Severe bruxism or clenching.
- Immunosuppressed or immunocompromised.
- Treated or under treatment with intravenous amino-bisphosphonates.
- Patients participating in other studies, if the present protocol could not be properly followed.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: computer guided screw holes locating guide and Patient Specific Champy plate osteosynthesis
the operation will under general anesthesia with nasal intubation and oral pack, Injection of 20 cc saline adrenaline 1:00000 to 0 in the sulcus for hemostasis, Vestibular mucosal incision, Reflect the flap to visualize the broken segments. Full thickness mucoperiosteal flaps were then carefully raised to expose enough underlying alveolar bone to accommodate the screw holes locating guide and the custom-made Champy plate. In Group I, Put the specific screw holes locating device in place and drill the screw holes, remove the screw holes locating device and mobilize the segments then apply the custom-made Champy plate and fix it with screw for passive reduction of the segments. Then suture the mucosa. |
the operation will under general anesthesia with nasal intubation and oral pack, Injection of 20 cc saline adrenaline 1:00000 to 0 in the sulcus for hemostasis, Vestibular mucosal incision, Reflect the flap to visualize the broken segments. Full thickness mucoperiosteal flaps were then carefully raised to expose enough underlying alveolar bone to accommodate the screw holes locating guide and the custom-made Champy plate. , Put the specific screw holes locating device in place and drill the screw holes, remove the screw holes locating device and mobilize the segments then apply the custom-made Champy plate and fix it with screw for passive reduction of the segments. Then suture the mucosa. |
|
Active Comparator: conventional Champy plate osteosynthesis in management of mandibular angle fracture
the operation will under general anesthesia with nasal intubation and oral pack, Injection of 20 cc saline adrenaline 1:00000 to 0 in the sulcus for hemostasis, Vestibular mucosal incision, Reflect the flap to visualize the broken segments. Full thickness mucoperiosteal flaps were then carefully raised to expose enough underlying alveolar bone then mobilize the broken segment, Arch bar was made to achieve proper occlusion put the Champy 2.0 plate on the ventral surface of the external oblique of the mandible and remove it for further bending using plate pliers for further accommodation of the plate then fix it in place using mono cortical screws. |
the operation will under general anesthesia with nasal intubation and oral pack, Injection of 20 cc saline adrenaline 1:00000 to 0 in the sulcus for hemostasis, Vestibular mucosal incision, Reflect the flap to visualize the broken segments.
Full thickness mucoperiosteal flaps were then carefully raised to expose enough underlying alveolar bone then mobilize the broken segment , Arch bar was made to achieve proper occlusion put the Champy 2.0 plate on the ventral surface of the external oblique of the mandible and remove it for further bending using plate pliers for further accommodation of the plate then fix it in place using mono cortical screws.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy of computer guided screw holes locating guide and Patient Specific Champy plate in management of mandibular angle fracture
Time Frame: 3 months
|
calculate any amount for segments deviation from the virtual plan in mms.
|
3 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0032025
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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