Study of Biomechanical Effects of Different Materials for Digitally Made Subperiosteal Implants on Severe Bone Loss in Upper Jaw
Led by Menoufia University · Updated on 2025-03-27
9
Participants Needed
1
Research Sites
9 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the biomechanical effects of digitally designed subperiosteal implants made from different materials on the atrophied upper jaw bone maxilla. These implants are considered for patients with advanced bone loss where traditional implants may not be suitable. The study aims to understand which implant material could be best suited for this condition, as there is limited evidence regarding the optimal material choice.
The study compares virtual designs of subperiosteal implant frameworks made from three materials titanium, PEEK, and PEKK. These frameworks are digitally constructed for use on the atrophied maxilla bone. A 3D image of the patients upper jaw bone is created from a computed tomography scan and processed into a digital model. This model is used to simulate force loading between the implant parts, screws, and bone tissues to analyze biomechanical behavior.
Participants will contribute by providing their computed tomography scan data that produces the 3D image of their edentulous maxilla bone. Researchers will analyze bone loss under the implants over a period of 10 to 15 years using digital simulation methods. The study is observational and does not involve direct treatment but focuses on evaluating implant framework materials and prosthetic superstructures in the digital environment. The trial includes adults aged 30 to 70 with specific bone classifications of the maxilla.
CONDITIONS
Brief Title
Biomechanical Effects of Digitally Constructed Subperiosteal Implants
Research Team
M
Mohammed A. El-Sawy, PhD
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A 3D image of an edentulous maxilla bone derived from a computed tomography scan of an adult patient.
Maxilla with Cawood and Howell class 4 or 5 classification
Age between 30 and 70 years
You will not qualify if you...
A 2D image of an edentulous maxilla bone
A non atrophied maxilla
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Diagnostic Evaluation
Duration - 1 day
Participants undergo a computed tomography (CT) scan to obtain a 3D image of the edentulous maxilla bone for virtual design analysis.
1 visit (in-person)
Monitoring
Duration - 10 to 15 years
Participants' virtual implant frameworks are analyzed to assess biomechanical effects and predict bone loss under the implants over time.
No in-person visits; observation based on virtual data
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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Published Research Related To This Trial
Biomechanical effects of digitally constructed titanium, modified polyetheretherketone, and polyetherketoneketone subperiosteal implants on atrophied maxilla: a finite element analysis.
Mohammed A El-Sawy, Basin El-Khatib, Hesham S Borg...