Ireland
--:--IST
Recruiting Not applicable

Virtual Lesion Segmentation and Mandibular Ameloblastoma Radiographic Safety Margin

NCT07306962 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-01-01
Last updated
2025-12-29

Condition(s) studied

Ameloblastoma

Investigational drug(s) / intervention(s)

Virtual lesion segmentation for mandibular ameloblastoma

Virtual lesion segmentation for mandibular ameloblastoma: Patient with mandibular ameloblastoma managed with virtual surgical planning \& Virtual lesion segmentation for the determination of a radiographic 10-mm safety margin.

Study summary

Reconstruction of segmental mandibular defects is in a continuous state of evolution utilizing the recent advances in Computer-Aided Designing (CAD) and preoperative Virtual Surgical Planning (VSP). The anterior iliac crest is one of the ideal reservoirs for autogenous harvesting of a bi-cortical bone block with 1:1 cortical to cancellous bone ratio which is optimal for rapid and predictable consolidation. The aim of this study is the utility of VSP guided by CT and confirmation by histopathological analysis in achieving negative margins and preventing recurrence of mandibular ameloblastoma.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Patients with histologically confirmed ameloblastoma using a preoperative biopsy. 2. Patients with ameloblastoma that require segmental mandibular continuity defect, not involving the condyle. Exclusion Criteria 1. Patients with lateral segmental mandibular defect involving the condyle. 2. Patients with an active infection at the site of resection. 3. Patients with recurrent lesion after resection.

Primary outcome measure(s)

  • Histological analysis and degree of lesion invasion determination — 1 month
    The specimen with the the mounted Safety Margin Calibration Guide will be sent for histological evaluation. For light microscopic examination, the specimens will be embedded in paraffin wax blocks after being fixed in 10% formalin, neutrally buffered, cleaned, and dehydrated using increasing ethanol concentrations. Tissue sections will be cut to a thickness of 4 μm, and stained with hematoxylin and eosin to be examined under a light microscope. The specimen will be cut, using the S35 (0.254-mm thickness) microtome blade, at the preoperatively determined margins according to the virtual lesion segmentation from the proximal and distal sides of the lesion. Since the study is limited to segmental mandibular resection, the full lower border of the mandible was resected and their will be no need for assessment of either coronal or apical margins

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry, Alexandria University Alexandria Alexandria Governorate Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07306962 on ClinicalTrials.gov ↗ ← All trials in Egypt