Actively Recruiting
Artificial Intelligence-Based Assessment of Endosseous Lesions
Led by University of Bari Aldo Moro · Updated on 2026-04-15
10
Participants Needed
2
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Despite these advances, CBCT interpretation remains largely qualitative and dependent on the clinician's experience. Conventional evaluation is based on two-dimensional slices and linear measurements, which may underestimate lesion complexity and spatial distribution. Recent developments in Artificial Intelligence in Medicine have introduced automated image segmentation tools capable of identifying lesion boundaries and calculating volumetric data. These technologies allow a transition from subjective assessment to objective, reproducible quantification. The potential clinical advantages include: * Objective measurement of lesion size (volume in mm³) * Improved surgical planning * Enhanced prediction of anatomical involvement * Reduction of diagnostic errors * Standardization of follow-up and outcome assessment Therefore, the aim of the present study was to evaluate the clinical impact of AI-based segmentation and volumetric analysis of endosseous lesions compared to conventional CBCT interpretation.
CONDITIONS
Official Title
Artificial Intelligence-Based Assessment of Endosseous Lesions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Good health according to the System of the American Society of Anesthesiology
- Aged older than 18 years
- No general medical contraindication for surgery
You will not qualify if you...
- Smoking more than 15 cigarettes a day
- Pregnancy
- Acute infections
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University of Bari Aldo Moro
Bari, Italy, 70021
Actively Recruiting
2
Dr. Giuseppe D'Albis
Bari, Italy, 70124
Actively Recruiting
Research Team
G
Giuseppe D'Albis, Dr.
CONTACT
S
Saverio Capodiferro, Prof.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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