Actively Recruiting

Age: 30Years - 70Years
All Genders
ID06362057

Biomechanical Effects of Digitally Constructed Subperiosteal Implants From Different Materials With Different Prosthetic Superstructures on Atrophied Maxilla: A Finite Element Analysis

Led by Menoufia University · Updated on 2025-03-27

9

Participants Needed

1

Research Sites

9 weeks

Total Duration

On this page

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 patient's 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

Who Can Participate

Age: 30Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • A 2D image of an edentulous maxilla bone
  • A non atrophied maxilla

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

Trial Site Locations

Total: 1 location

1

Mohammed A. El-Sawy

Al Mansurah, Egypt, 12345

Actively Recruiting

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Research Team

M

Mohammed A. El-Sawy, PhD

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...

https://pubmed.ncbi.nlm.nih.gov/40640731