Patient Specific Plates Versus Conventional Miniplates for Treatment of Mandibular Body Fractures
Primary Purpose
Mandibular Fractures
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Computer guided patient specific 3D titanium plate
Conventional titanium miniplates
Sponsored by
About this trial
This is an interventional treatment trial for Mandibular Fractures
Eligibility Criteria
Inclusion Criteria:
- Patients with unilateral mandibular body fractures, not associated with other mandibular and maxillofacial fractures
Exclusion Criteria:
- Patients with bilateral mandibular fractures
- Patients with other mandibular or maxillofacial fractures
- Comminuted fractures
- Medical problem that may interfere with the procedure such as bleeding disorder and pregnancy.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control Arm
Intervention arm
Arm Description
Conventional titanium miniplates
Patient specific 3D plates
Outcomes
Primary Outcome Measures
Patient Satisfaction measured with visual analogue scale (0-10)
patient satisfaction is defined as patient-reported outcome measure while the structures and processes of care can be measured by patient-reported experiences (30). Measured on a visual analogue scale (VAS) (29) of 0-10 ,with zero being unsatisfied and 10 being satisfied. Patient Satisfaction is assessed regarding prescence of pain, occlusal discrepencies and overall patient satisfaction.
Secondary Outcome Measures
Fracture gap distance
This is done using CBCT through measuring the fracture gap distance in millimeters to evaluate proper reduction and fixation
Occlusal bite force
The biting force will be measured through the follow up visits (1 week,3 months) by the bite force recorder at the incisor region, right and left molar region. The measurement of the bite force will be undertaken using a portable type of occlusal force gauge (GM10, Nagano Keiki, Japan) called OCCLUSAL FORCE-METER GM10. (36)
Operating time
The time of the surgery will be recorded using a stopwatch.
Plate palpability
Measured during all follow up visits, by questioning the patient ,where the patient will be informed of the site of the plates ,and asked if he feels the plates are palpable ,and will be measured by binary measuring unit (yes/no) , also the plates will be palpated by the operator at follow up visits.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03608891
Brief Title
Patient Specific Plates Versus Conventional Miniplates for Treatment of Mandibular Body Fractures
Official Title
Patient Specific Three-Dimensional Titanium Plates Versus Conventional Miniplates for Treatment of Mandibular Body Fractures. (Randomized Clinical Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 2018 (Anticipated)
Primary Completion Date
February 2019 (Anticipated)
Study Completion Date
July 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the current study is to evaluate and assess the clinical stability and efficacy of patient specific computer guided titanium plates versus the conventional titanium mini plates regarding accurate reduction and fixation of mandibular body fractures, reducing the operating time, achieving precise bone alignment and reducing the plate palpability.
Detailed Description
The study will be conducted on two groups:
Intervention group: patient specific three-dimensional titanium plates CBCT or CT scan will be performed for the patient, the dicom files will be imported into a surgical planning software , plates will then be designed virtually and sent for three-dimensional (3D) printing.
Control group: Conventional miniplates:
In this group two miniplates of titanium Mini-System 2.0 mm will be used. The plate has profile height 1.0 mm whereas the screw length varies according to the site of the plate. According to Champy osteosynthesis lines for fixation of the posterior mandibular fracture ,the first plate will be placed at the inferior border from the buccal side, using bicortical screws engaging the buccal and lingual cortices to achieve rigid fixation, while the second plate will be placed at about 5mm superior to the inferior plate in the subapical region, using monocortical screws engaging only the buccal cortex to avoid injuring the teeth roots.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mandibular Fractures
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control Arm
Arm Type
Active Comparator
Arm Description
Conventional titanium miniplates
Arm Title
Intervention arm
Arm Type
Experimental
Arm Description
Patient specific 3D plates
Intervention Type
Device
Intervention Name(s)
Computer guided patient specific 3D titanium plate
Other Intervention Name(s)
Intervention Arm
Intervention Description
CBCT or CT scan will be done preoperatively and dicom files will be imported to mimics software to design and print the patient specific 3D titanium plate.
Intervention Type
Device
Intervention Name(s)
Conventional titanium miniplates
Other Intervention Name(s)
Control arm
Intervention Description
In this group two miniplates of titanium Mini-System 2.0 mm will be used. The plate has profile height 1.0 mm whereas the screw length varies according to the site of the plate. According to Champy osteosynthesis lines for fixation of the posterior mandibular fracture ,the first plate will be placed at the inferior border from the buccal side, using bicortical screws engaging the buccal and lingual cortices to achieve rigid fixation, while the second plate will be placed at about 5mm superior to the inferior plate in the subapical region, using monocortical screws engaging only the buccal cortex to avoid injuring the teeth roots.
Primary Outcome Measure Information:
Title
Patient Satisfaction measured with visual analogue scale (0-10)
Description
patient satisfaction is defined as patient-reported outcome measure while the structures and processes of care can be measured by patient-reported experiences (30). Measured on a visual analogue scale (VAS) (29) of 0-10 ,with zero being unsatisfied and 10 being satisfied. Patient Satisfaction is assessed regarding prescence of pain, occlusal discrepencies and overall patient satisfaction.
Time Frame
Measured immediately after the surgery
Secondary Outcome Measure Information:
Title
Fracture gap distance
Description
This is done using CBCT through measuring the fracture gap distance in millimeters to evaluate proper reduction and fixation
Time Frame
0 and 3 months
Title
Occlusal bite force
Description
The biting force will be measured through the follow up visits (1 week,3 months) by the bite force recorder at the incisor region, right and left molar region. The measurement of the bite force will be undertaken using a portable type of occlusal force gauge (GM10, Nagano Keiki, Japan) called OCCLUSAL FORCE-METER GM10. (36)
Time Frame
0 and 3 months
Title
Operating time
Description
The time of the surgery will be recorded using a stopwatch.
Time Frame
time of the surgery
Title
Plate palpability
Description
Measured during all follow up visits, by questioning the patient ,where the patient will be informed of the site of the plates ,and asked if he feels the plates are palpable ,and will be measured by binary measuring unit (yes/no) , also the plates will be palpated by the operator at follow up visits.
Time Frame
0 and 3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients with unilateral mandibular body fractures, not associated with other mandibular and maxillofacial fractures
Exclusion Criteria:
Patients with bilateral mandibular fractures
Patients with other mandibular or maxillofacial fractures
Comminuted fractures
Medical problem that may interfere with the procedure such as bleeding disorder and pregnancy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dina A Alei El Dine, Postgraduate
Phone
01285568850
Email
dinaadelta3lab@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed A Farid, PHD
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohamed A Abd el Rasol, PhD
Organizational Affiliation
Cairo University
Official's Role
Study Chair
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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22655117
Citation
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Citation
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Citation
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Citation
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Patient Specific Plates Versus Conventional Miniplates for Treatment of Mandibular Body Fractures
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