Computer Guided for Mandibular Distraction Osteogenesis
NCT ID: NCT03869021
Last Updated: 2019-03-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
12 participants
INTERVENTIONAL
2015-12-30
2018-12-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: The study presents computer-guided distraction osteogenesis surgery using prefabricated splints.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Digital Occlusal Wafer Versus Waferless Distal Segment Repositioning for BSSO in Skeletal Mandibular Deformities
NCT05151042
Evaluation of Effect of Bone Marrow Aspirate Concentrate on Distracted Mandibular Bone Properties
NCT03861650
Guided Biaxial Alveolar Distraction Device in Posterior Atrophic Mandible
NCT05602909
Radiographic Assessment Of The Accuracy Of 3D Ridge Augmentation In Anterior Mandible Using Computer Guided Autogenous Cortical Shell Technique Versus Free Hand Technique
NCT06691516
Measuring the Influence of Maxillary Obturator Prosthesis on Facial Morphology in Patient With Unilateral Maxillary Defects Using Stereophotogrammetry
NCT05310149
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Each patient was positioned in the machine and imaged at the same manner according to the recommendations of CBCT manufacturer. The Frankfurt plane was positioned parallel to the horizontal plane and the midsagittal plane was perpendicular to the horizontal plane.
The CBCT scan was required to fulfill the following criteria:
* Showing the full bony facial structures, extending from at least the inferior border of the mandible to the supraorbital ridge.
* CBCT scan should be free from any motion artifacts.
* Patient biting on cotton rolls in order to free the occlusion.
* A scan of optimum quality and resolution. (0.25 mm voxel size) IV. Virtual Treatment Planning
* The data from the CBCT scan were exported from the i-CAT Vision software in DICOM format, which was in turn imported into Mimics Medical 19.0 software (Materialise NV, Technologielaan 15, 3001 Leuven, Belgium) for virtual treatment planning.
* Using the "Thresholding" tool, the range of gray value sets is chosen to highlight the mineralized structures and separate them from the rest of soft tissue structures in the scan creating a new mask.
* Using the "Calculate 3D" tool on the new mask, a 3D rendering of the facial mineralized structures is created and is then refined using the "Smoothing" and "Wrap" tools.
* In order to properly orient the patient's head position, analyze the deficiencies, and standardize the planning process, the Frankfort Horizontal plane and the Midsagittal plan were constructed. Frankfort Horizontal Plane was defined by marking the right and left Orbitale, and the Porion of the non-affected side. The Midsagittal plane was defined by marking the Sella, the Nasion, and the Anterior Nasal Spine.
* Using the "Multiple Slice Edit" and "Region Growing" tools when needed, the jaws are separated and the mandible and maxilla are segmented separately.
* Using the "Distraction Wizard", an appropriate distraction type is selected. A distractor is selected and placed on the proposed site for distraction. The osteotomy and vector are visualized and the distractor is activated. This process is repeated until the final outcome is satisfactory. The ideal final outcome is when the canted occlusal plane is corrected and the mandibular midline is coincident with the facial midline simultaneously.
* Using the "Cylinder" tool in the "Medcad" menu, virtual distractor pins and osteotomy disk are drawn to match our selected custom-made distractor. The number of pins, their size, and orientation differed according to the vital structures in each distraction site. Hence, custom-made distractors were used. Guide fixation screws are also added to provide further retention for the guide when needed. The fixation screws, osteotomy and distractor pins are placed so as to avoid injury to any vital structures as the Inferior Alveolar Nerve, tooth buds, and dental roots .
* Using different Boolean operation, the body of the final guide is designed to fit over the bones and teeth and incorporate the different distractor components. It is then exported into STL format.
* The exported STL file is printed with Formlabs Form 2 stereolithography (SLA) 3D printer (Formlabs Inc. Somerville, MA 02143 USA) using Clear Photopolymer resin (FLGPCL02). The finished printed model is then checked for fit with the distractor.
* Prior to surgery, the guide is submerged in a basin containing 2.4% activated glutaraldehyde solution (Cidex) for 20 minutes for high level disinfection.
Surgical Procedure
* The patient was placed in supine position. General anesthesia was administered through Naso-Tracheal intubation. A cannula was inserted in a peripheral vein (18G) and normal saline infusion was started at a rate of 6 ml/kg along with Ringer's solution.
* Anesthesia was induced with IV propofol 1.5-2 mg/kg, fentanyl 1.3 μ/kg and succinyl choline 1mg/kg to facilitate nasotracheal intubation using armored tube. Anesthesia was maintained with isoflurane in oxygen and atracurium in a dose of 0.3-0.6 mg/kg.
* The surgical sites were prepared with povidone iodine and then draped according to the standard oral and maxillofacial surgery operating room procedures.
* An Antibiotic dose of 1 gm Cefotaxime vial was administered followed by Dexamethasone phosphate (as sodium salt) 4 mg vial through peripheral IV route at the beginning of the procedure. A local anesthetic solution of Articaine 4% containing Epinephrine (1:200,000) was infiltrated along the proposed operative field for hemostasis.
* A three-line pyramidal incision was performed. The distal incision was carried buccally across the external oblique ridge, and then joined to a gingival incision running buccally around the necks of the teeth on which the guide rests. The releasing incision is carried in a curved manner inferiorly and anteriorly, keeping in mind not to extend to the area of the mental foramen. Reflection of the flap was done with a periosteal elevator beginning from under the periosteum of the anterior buccal incision, working parallel to the gingival margin to detach the papillae and push distally.
* Once the field of interest was exposed, the guide was introduced onto the bone and teeth, and moved until a tight fit was achieved throughout its fitting surface. When needed, the guide was secured to the underlying bones by 2.0 miniscrews placed through their preplanned guiding tubes.
* Via a small stab incision through the skin, a transbuccal trochar is introduced, through which the self-drilling extraoral distractor pins are passed. The pins are inserted into the mandible at their designated points of entry through the guide.
* Using a piezotome, the osteotomy line is marked and the osteotomy is initiated guided by the osteotomy slit in the guide. The fixating screws and the guide are then removed. The use of piezotome allowed the planning of the osteotomies through the path of the inferior alveolar nerve without fear of nerve injury.
* After guide removal, the osteotomy is completed. The distractor is connected to the extraoral distractor pins and is then activated to insure free mobility of the distal segment. Once confirmed, the distractor is returned to its zero position. The flap was then repositioned and closed using 4-0 Braided Polyglycolic Acid sutures.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Computer guided surgery
A surgical guide is 3d printed to guide through the surgery, the patients of this group will have the distraction surgery by a guide designed by Mimics 19.0, Materialise NV,Belgium
3D printed surgical guide constructed
A printed surgical guide ( to direct through the surgery and make results predictable), the guide is designed by Mimics 19.0, Materialise NV,Belgium and printed with self cure resin
No surgical guide (free hand surgery)
control group added to investigate the effect of surgical guide
free hand surgery
A control group in which patients are randomly assigned and surgeries are planned without surgical guides and performed free handed
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
3D printed surgical guide constructed
A printed surgical guide ( to direct through the surgery and make results predictable), the guide is designed by Mimics 19.0, Materialise NV,Belgium and printed with self cure resin
free hand surgery
A control group in which patients are randomly assigned and surgeries are planned without surgical guides and performed free handed
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Patients younger than 25 years old.
3. Patients included in the study were hemifacial microsomia
4. Distraction range was between 15-20 mm.
Exclusion Criteria
2. Previous radiotherapy on head and neck region.
3. Chemotherapy within the past 12-month period.
4. An active infection at the distraction site.
5 Years
25 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Yasser Mohamed Nabil Ahmed Khirat El Hadidi
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yasser Mohamed Nabil Ahmed Khirat El Hadidi
Assistant Lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
yasser el hadidi, mds
Role: PRINCIPAL_INVESTIGATOR
Ain Shams University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ain shams university
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
392B
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.