Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Evaluation of Different Color Determination Methods

19 augusti 2026 uppdaterad av: Mehmet Gözen, Konya Necmettin Erbakan Üniversitesi

In Vivo Evaluation of Different Color Determination Methods for Accuracy and Reproducibility

With the increasing aesthetic demands in dental practice, the accuracy and consistency of tooth color determination methods have gained importance for clinical success. This study aims to compare different tooth color determination methods in terms of accuracy and repeatability under in vivo conditions. A spectrophotometric system (VITA Easyshade V) will be used as the reference method. In comparison, the results obtained through visual assessment by observers, a digital intraoral scanner (TRIOS 3), and artificial intelligence-based color analysis systems will be evaluated. Statistical analyses will be conducted based on ΔE, L*, a*, b*, and shade code data obtained from the measurements, and the agreement among the methods as well as their correlations with the spectrophotometer will be examined. This study aims to demonstrate the clinical validity of digital and AI-assisted methods and to emphasize the importance of objective approaches in tooth shade selection.

The aim of this study is to compare four different tooth color determination methods used in aesthetic dentistry-spectrophotometric system, observer-based visual assessment, digital intraoral scanner, and artificial intelligence-assisted analysis system-in terms of accuracy and repeatability under in vivo conditions. The study seeks to statistically evaluate and compare the color measurement values obtained from these methods with those of the spectrophotometric system, which is considered the reference method, and to determine the level of agreement among the methods. In addition, it aims to assess the clinical applicability and reliability of digital technologies and artificial intelligence-based systems in tooth color selection.

Studieöversikt

Detaljerad beskrivning

This analytical cross-sectional clinical study was conducted between May 2025 and June 2025 at the Department of Prosthodontics, Faculty of Dentistry, Necmettin Erbakan University. The study aims to demonstrate the clinical validity of digital and artificial intelligence-assisted methods and to contribute to emphasizing the importance of objective approaches in tooth shade selection.

A total of 40 adult participants with healthy maxillary central incisors were included in the study.

Color measurements will be taken from the middle third of the labial surface of each participant's maxillary central incisor. All measurements will be performed by the same clinician, in a fixed position, and under standardized lighting conditions.

Color Determination Methods:

  1. Spectrophotometric Measurement:

    The VITA Easyshade V spectrophotometer will be used as the reference method. The device will be calibrated before each use, and measurements will be taken in a perpendicular position to the tooth surface. VITA 3D Master shade values as well as L*, a*, and b* parameters will be recorded.

  2. Visual Assessment:

    Observer-based visual evaluation will be performed using the VITA 3D Master shade guide. To minimize visual bias, the evaluation time will be limited to 10 seconds, and the selected shade values will be converted into the CIE Lab* color system.

  3. Digital Intraoral Scanner:

    The TRIOS 3 digital intraoral scanner will be used for image acquisition following device calibration. The color values obtained from the scans will be recorded.

  4. Artificial Intelligence-Assisted Color Analysis:

Photographs of the teeth will be taken in RAW format under natural light, from a fixed distance, and against a neutral gray background. After preprocessing, the images will be analyzed using a specially trained image-processing model based on artificial intelligence.

Data Analysis:

The color values obtained from each method will be compared with those from the spectrophotometric measurements. Color differences will be calculated using the ΔE formula. One-way ANOVA and Bonferroni post-hoc tests will be employed to evaluate differences among the methods. The agreement between L*, a*, and b* values will be analyzed using Kendall's tau-b correlation analysis, while the consistency of shade code matching will be assessed using Cohen's Kappa statistics. All data will be processed and evaluated using an appropriate statistical analysis software program.

Studietyp

Observationell

Inskrivning (Faktisk)

40

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Selçuklu
      • Konya, Selçuklu, Turkiet (Türkiye), 42090
        • Necmettin Erbakan University

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen

Tar emot friska volontärer

Ja

Testmetod

Icke-sannolikhetsprov

Studera befolkning

The study was conducted on 40 adult participants with healthy maxillary central incisors. Color measurements were obtained from the middle third of the labial surface of each participant's respective tooth, under standardized lighting conditions and in a fixed position, by the same clinician. All participants were voluntarily recruited from patients who applied to the Department of Prosthodontics, Faculty of Dentistry, Necmettin Erbakan University.

Beskrivning

Inclusion Criteria:

  • Age 18 years or older
  • Absence of restorations, discoloration, or structural defects on the maxillary central incisors
  • Willingness to undergo digital measurement and clinical evaluation

Exclusion Criteria:

  • Presence of restorations or discoloration on the anterior teeth
  • Existence of structural defects, malposition, or enamel hypoplasia
  • History of orthodontic or prosthodontic treatment
  • Individuals with systemic diseases or a history of psychiatric or neurological disorders

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Spectrophotometric Shade Selection
Tidsram: baseline
After calibration according to the manufacturer's instructions, the spectrophotometer will be used to determine the shade from the middle third of the maxillary central incisor. The color difference between the L*, a*, and b* values obtained from each group and the reference measurement will be calculated using the CIEDE2000 (ΔE00) formula.
baseline

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

7 maj 2025

Primärt slutförande (Faktisk)

7 maj 2025

Avslutad studie (Faktisk)

13 juni 2025

Studieregistreringsdatum

Först inskickad

19 augusti 2026

Först inskickad som uppfyllde QC-kriterierna

19 augusti 2026

Första postat (Faktisk)

24 augusti 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

24 augusti 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

19 augusti 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • Neu2025

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

OBESLUTSAM

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera