Enrolling by invitation NCT06972797

Accuracy of 3D Slicer Software for Automatic Segmentation Versus Manual Segmentation Using Commercial Software to Evaluate Impacted and Unerupted Maxillary Canine: An Observational Study

— Observational Impacted Canines

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to: Registry conditions: Impacted Canines. Basic parameters: 8 years — 70 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Egypt
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Accuracy of the DentalSegmentator Tool in 3D Slicer Software Compared to Manual Segmentation in Romixes Software in the Evaluation of Unerupted and Impacted Maxillary Canine: An Observational Study

Overview

Our research question will be, can automatic segmentation of maxillary impacted and unerupted canine using DentalSegmentator tool in 3D silcer software be as accurate as manual segmentation?

Primary outcome measures

3D volume analysis [Time frame: one year]

Eligibility criteria

Inclusion criteria

Age ranges from 8-70y (from 8 to less than15y for unerupted group - from 15 to 70y for impacted group). b. Scans clearly showing unerupted and impacted maxillary canines.

Exclusion criteria

Scans with artifacts obscuring the area of interest.
Scans with fractures or pathological lesions obscuring the area of interest.
Image blurring due to patient movement during acquisition which could interfere with image interpretation.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Other

Study locations

Egypt · 1 center

Cairo university- faculty of dentistry — Cairo

Identifiers

NCT: NCT06972797 · CairoU_REC IM031839

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗