Effects of digitally made subperiosteal implants on bone loss

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the biomechanical effects of subperiosteal implants constructed using digital technology. It focuses on patients with advanced bone atrophy in the maxilla, utilizing 3D imaging from computed tomography scans to assess the suitability of various materials for implant fabrication. The study aims to provide insights into the effectiveness of these implants in treating bone loss, particularly in cases classified as Cawood and Howell class 4 or 5.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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

Exclusion Criteria:

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

Where it's running

• Mohammed A. El-Sawy
  Al Mansurah, Egypt Recruiting

Study contacts

• Study coordinator: Mohammed A. El-Sawy, PhD
• Email: Dr_sawy@windowslive.com
• Phone: 161314522

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.