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Evaluation of the Scanning Accuracy of Scanners Operating With Different Scanning Technologies in Mandibular and Maxillary Edentulous Ridges

NCT07209826 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-04-10
Last updated
2025-10-07

Condition(s) studied

AccuracyMeasurement Reliability

Investigational drug(s) / intervention(s)

Trios 5iTero LuminaMedit i700E4 Lab Scanner

Trios 5: Each patient's edentulous ridges are planned to be scanned three times with Trios 5.To ensure optimum accuracy, scans were performed in a standard dark environment in accordance with the manufacturer's scanning protocols.

iTero Lumina: Each patient's edentulous ridges are planned to be scanned three times with iTero Lumina.To ensure optimum accuracy, scans were performed in a standard dark environment in accordance with the manufacturer's scanning protocols.

Medit i700: Each patient's edentulous ridges are planned to be scanned three times with Medit i700.To ensure optimum accuracy, scans were performed in a standard dark environment in accordance with the manufacturer's scanning protocols.

E4 Lab Scanner: Conventional measurements will be taken from each patient, and the resulting master model (reference scan) will be scanned using an industrial scanner with high scanning accuracy (E4 lab scanner, 3shape, Denmark) to obtain digital data.

Study summary

This study aims to evaluate the scanning accuracy of scanners equipped with Active Triangulation, Confocal Microscopy, and Multi-Direct-Capture technologies.

Department of Prosthetic Dentistry, Faculty of Dentistry, Ege University , 30 patients who applied for a complete removable denture and met the inclusion criteria will have conventional impressions taken. The resulting master model (reference scan) will be scanned using an industrial scanner with high scanning accuracy (E4 lab scanner, 3shape, Denmark) to obtain digital data. Edentulous ridges; Active Triangulation (Medit i700, Seoul, South Korea), Confocal Microscopy (Trios 5, Henry Schein Dental, Gillingham, Kent, UK), and Multi-Direct-Capture technologies (iTero Lumina, Align Technologies, San Jose, California, USA) will be scanned three times using the scanning protocols recommended by the manufacturers and digitized. All digital data obtained will be evaluated using Geomagic (Studio 2015; 3D Systems Inc., Darmstadt, Germany) 3D analysis software to match the reference data and verify its accuracy according to the accepted reference measurement.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Individuals aged 18 to 80 * Upper and lower edentulous ridges * Individuals who have not received radiation therapy or chemotherapy * Individuals who have not been diagnosed with dry mouth * Individuals without active mouth sores due to systemic diseases * Patients who accept the study conditions will be included in the study. Exclusion Criteria: * Patients whose extraction site has not yet healed or whose last tooth extraction was less than 2 months ago * Individuals who have undergone radiation therapy and chemotherapy * Individuals diagnosed with dry mouth * Individuals with active mouth sores due to systemic diseases * Patients who do not agree to the study conditions will not be included in the study.

Primary outcome measure(s)

  • Accuracy of Intraoral Scanners Compared With Reference Extraoral Scanner — Two months
    The primary outcome is the trueness (accuracy) of three intraoral scanners (Trios 5, Medit i700, iTero Lumina) in capturing edentulous maxillary and mandibular arches. Accuracy will be assessed by comparing the surface deviation of intraoral scan data to the reference dataset obtained from the extraoral laboratory scanner of a conventional stone cast. Mean root-mean-square (RMS) error values (measured in micrometers, µm) will be calculated for each scanner relative to the reference to quantify the deviation.

Trial sites (1)

FacilityCityRegionStatus
Ege University,Faculty of Dentistry,Department of Prosthodontics,Izmir Izmir Turkey (Türkiye)
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 NCT07209826 on ClinicalTrials.gov ↗ ← All trials in Turkey