Evaluation of Using 3D Printed PEEK Facial Implants in Repairing Maxillofacial Deformities

Sponsor
Tishreen University (Other)
Overall Status
Completed
CT.gov ID
NCT05348434
Collaborator
(none)
10
1
25.5
0.4

Study Details

Study Description

Brief Summary

Objective: Evaluation of using 3D printed polyether ether ketone facial implants in repairing maxillofacial deformities.

Research materials and methods: The research sample consisted of 10 patients with facial deformities (maxillofacial trauma patients with hard tissue deficiencies, tumor patients who had previous facial surgery, patients have retrognathia, congenital malformation, patients with hemifacial microsomia - bone loss as a result of a mucormycotic infection or black fungus ) Between 2020 and 2021 in the Department of Oral and Maxillofacial Surgery in the Tishreen University Hospital - Latakia - Syria. All patients underwent Computed Tomography (CT) scans under the condition of providing a large number of slices (more than 200 slices) per axis, and the thickness of each slice is less than 1 mm with 64-bit resolution, Then the design of the required facial implant was carried out in coordination between the designer and the surgical team. The final form of the facial implant was printed from PolyEther Ether Ketone (PEEK), and then surgical work was performed for patients under general anaesthetic according to the appropriate surgical entrance. The implants were fixed in place using titanium screws and the patients were given appropriate pharmacological coverage .

Condition or Disease Intervention/Treatment Phase
  • Procedure: 3D printed polyether ether ketone facial implants in repairing maxillofacial deformities

Detailed Description

10 patients with maxillofacial deformities (trauma patients, war injuries, patients with pre-existing maxillofacial tumours, and mucormycotic patients) for reconstruction with 3D printed facial implants made of PEEK, between 2020 and 2021 in the Department of Oral and maxillofacial Surgery at the Tishreen University Hospital, Latakia, Syria. All patients underwent three-axial CT scan using a Toshiba Slice CT Scanner-Imaging, under the condition of providing a large number of slices (more than 200 slices) per axis, and the thickness of each slice is less than 1 mm with 64-bit resolution. Representative models of patient anatomical data were created based on the radiated raw data of the patient obtained via Digital Imaging and Communications in Medicine (DICOM) from the CT scan. The DICOM format is 0.3 to 0.6 mm thick, depending on the anatomical region. The medical modelling software (EXoCad) was used to compile DICOM data at the axial, sagittal, and coronal planes and then create a 3D virtual model of the anatomical region.

The surgeon and the manufacturing technician met to discuss the design format and any modifications required, with the proposed areas for placement of the titanium screws for the installation of the facial implant. The final default model for the facial implant was exported as a STereoLithography (STL) file and sent to the 3D printer, which was eventually made for the patient. The printer used in our study is a prototype of OO-Kuma Katana HT PEEK 3D Printer. After the process of printing, the facial implant is steam sterilized and then the implant is encapsulated. The surgical work of the patients was performed under general anaesthesia at the Tishreen University Hospital, Latakia, Syria, at the appropriate surgical entrance depending on the size and location of the deformity. The facial implant was checked to be suitable before stabilization and the required modifications were made during the process. The PSI was fixed in place using 1.5 to 2.0mm sized titanium screws, all patients received an intravenous 1.2g Augmentin dose and 0.5g of Flagyl during the procedure. After the surgery, patients received two doses of Augmentin, after which a prescription of Augmentin 1g and Flagyl 0.5g orally per day for a week was given.

Study Design

Study Type:
Observational
Actual Enrollment :
10 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Using 3D Printed Polyether Ether Ether Ketone Facial Implants in Repairing Maxillofacial Deformities
Actual Study Start Date :
Feb 25, 2020
Actual Primary Completion Date :
Mar 5, 2022
Actual Study Completion Date :
Apr 10, 2022

Arms and Interventions

Arm Intervention/Treatment
patients with maxillofacial deformities

10 patients with maxillofacial deformities (trauma patients, war injuries, patients with pre-existing maxillofacial tumours, and meucrmycotic patients)

Procedure: 3D printed polyether ether ketone facial implants in repairing maxillofacial deformities
All patients underwent Computed Tomography (CT) scans under the condition of providing a large number of slices (more than 200 slices) per axis, and the thickness of each slice is less than 1 mm with 64-bit resolution, Then the design of the required facial implant was carried out in coordination between the designer and the surgical team. The final form of the facial implant was printed from PolyEther Ether Ketone (PEEK), and then surgical work was performed for patients under general anaesthetic according to the appropriate surgical entrance. The implants were fixed in place using titanium screws
Other Names:
  • PSI PEEK
  • Outcome Measures

    Primary Outcome Measures

    1. Evaluation of Cosmetic patients' satisfaction level . [after 3 months of the surgical procedure]

      Three months after the surgery, we asked the patient to evaluate the aesthetic result by choosing a number from 1 to 5 , as 5 is the best cosmetic result. satisfaction scale : bad medium neutral satisfied very satisfied

    2. Evaluation of infection after using 3D printed polyetheretherketone facial implants in repair of maxillofacial deformities [after surgical procedure a week, one month and three months]

      A doctor _not included in the research team_ performed clinical examinations of patients after surgical procedure a week, one month and three months to check for clinical signs of infection . When there are signs of infection, he records the number 1 . When there are no signs of infection, he records the number 0 .

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • patients with facial deformities:
    1. maxillofacial trauma patients with hard tissue deficiencies

    2. tumor patients who had previous facial surgery

    3. patients have retrognathia

    4. congenital malformation

    5. patients with hemifacial microsomia

    6. bone loss as a result of a mucormycotic infection or black fungus

    Exclusion Criteria:
    1. acute stage oncology patients

    2. There is not enough soft tissue to cover the facial implants

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tishreen university Latakia Syrian Arab Republic

    Sponsors and Collaborators

    • Tishreen University

    Investigators

    • Study Chair: Hekmat Yacoub, PHD, Tishreen University
    • Study Director: Ali Khalil, PHD, Tishreen University
    • Principal Investigator: Ahmad Ahmad, Master, Tishreen University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tishreen University
    ClinicalTrials.gov Identifier:
    NCT05348434
    Other Study ID Numbers:
    • Tishreen U- Maxillofacial sur
    First Posted:
    Apr 27, 2022
    Last Update Posted:
    Apr 27, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Tishreen University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 27, 2022