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Comparison of Digital Analysis and Artificial Intelligence for Cephalometric Tracing
17 juni 2026 bijgewerkt door: Andrea Scribante, University of Pavia
Cephalometric Tracing: A Comparison Between Digital Analysis and Artificial Intelligence
This study aims to evaluate the accuracy and reliability of artificial intelligence (AI)-based cephalometric analysis compared with digital manual tracing.
A total of 100 standardized lateral cephalometric radiographs will be analyzed using Delta-Dent software with manual landmark identification and three fully automated AI-based systems (WebCeph, QuantX, and Smartee).
Sagittal, vertical, dental, and soft tissue cephalometric parameters will be compared among the different methods.
Statistical analysis will assess inter-method agreement and the clinical relevance of any observed discrepancies.
The study seeks to determine whether AI-based systems provide measurements comparable to conventional digital tracing and whether they can be considered reliable adjunctive tools in orthodontic diagnosis and treatment planning.
Studie Overzicht
Toestand
Werving
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This prospective observational study aims to evaluate the accuracy, reproducibility, and clinical reliability of artificial intelligence (AI)-based cephalometric analysis systems compared with digital manual tracing.
Patients whose lateral cephalometric radiographs were previously acquired for orthodontic diagnostic purposes at the Unit of Orthodontics and Paediatric Dentistry, University of Pavia, will be retrospectively selected according to predefined inclusion and exclusion criteria.
Written informed consent for the use of clinical records for research purposes will be obtained from all participants or their legal guardians.
A total of 100 standardized digital lateral cephalometric radiographs will be included in the study.
Each radiograph will be analysed using Delta-Dent software with manual landmark identification and three fully automated AI-based software systems: WebCeph™, QuantX, and Smartee.
Cephalometric analyses will be performed without manual adjustment of landmarks in the AI-based systems.
Ten cephalometric parameters representative of sagittal, vertical, dental, and soft tissue relationships will be evaluated, including SNA, SNB, ANB, SN-GoGn, L1-GoGn, U1-ANSPNS, nasolabial angle, facial angle, Wits appraisal, and N-Me.
Manual digital tracing performed by a single experienced orthodontist will be considered the reference method.
Intra-rater reliability will be assessed using intraclass correlation coefficient (ICC).
Statistical analysis will be conducted using R software (version 3.1.3;
R Foundation for Statistical Computing, Wien, Austria).
Descriptive statistics will be calculated for all variables.
Normality of data distribution will be assessed using the Kolmogorov-Smirnov test.
Comparisons among the different methods will be performed using the Friedman test followed by Dunn's post hoc test.
Statistical significance will be predetermined at p < 0.05.
Studietype
Observationeel
Inschrijving (Geschat)
100
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Andrea Scribante, DDS, PhD
- Telefoonnummer: +39 0382516223
- E-mail: andrea.scribante@unipv.it
Studie Locaties
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Italy
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Pavia, Italy, Italië, 27100
- Werving
- Unit of Orthodontics and Pediatric Dentistry - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Pediatrics - University of Pavia, Pavia, Lombardy 27100
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Contact:
- Andrea Scribante, DDS, PhD
- Telefoonnummer: +39 0382516223
- E-mail: andrea.scribante@unipv.it
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-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Bemonsteringsmethode
Niet-waarschijnlijkheidssteekproef
Studie Bevolking
The study population consists of patients of any age and sex who underwent digital lateral cephalometric radiography as part of routine orthodontic diagnostic records at the Unit of Orthodontics and Paediatric Dentistry, University of Pavia.
Radiographs meeting the predefined inclusion and exclusion criteria will be retrospectively selected for analysis.
Beschrijving
Inclusion Criteria:
- Availability of digital lateral cephalometric radiographs of adequate diagnostic quality
- Radiographs acquired with patients in centric occlusion and proper head positioning using a cephalostat
- Patients of any age and sex
- Absence of congenital or acquired craniofacial anomalies
- No previous orthodontic treatment
- No previous orthognathic surgical treatment
- Absence of agenesis of incisors or first molars
- Absence of supernumerary teeth overlapping the region of interest
Exclusion Criteria:
- Radiographs presenting artifacts or inadequate visualization of anatomical structures
- History of significant craniofacial trauma
- Radiographs acquired without a cephalostat
- Presence of severe skeletal asymmetries
- Incomplete clinical or radiographic records
- Radiographs unsuitable for manual or AI-based cephalometric landmark identification
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
|---|---|
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Orthodontic Patients with Lateral Cephalometric Radiographs
This study includes a single observational arm, since all lateral cephalometric radiographs included in the study will undergo the same analysis procedures.
Each radiograph will be evaluated using one digital manual tracing method (Delta-Dent) and three fully automated artificial intelligence-based cephalometric analysis systems (WebCeph™, QuantX, and Smartee).
No patient allocation, randomization, or therapeutic intervention will be performed.
|
All included lateral cephalometric radiographs will undergo cephalometric analysis using both digital manual tracing and artificial intelligence-based automated systems.
Manual digital tracing will be performed with Delta-Dent software by a single experienced orthodontist through manual identification of cephalometric landmarks.
The same radiographs will subsequently be analysed using three fully automated AI-based software programs (WebCeph™, QuantX, and Smartee) without manual correction of landmark positioning.
No therapeutic intervention or modification of patient treatment will be performed, as this is an observational comparative study based exclusively on retrospective analysis of radiographic records.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Agreement between AI-based cephalometric analysis and digital manual tracing
Tijdsspanne: Baseline
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Agreement between cephalometric measurements obtained with AI-based software systems and digital manual tracing will be assessed using the intraclass correlation coefficient (ICC) and differences in angular and linear cephalometric measurements.
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Baseline
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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SNA
Tijdsspanne: Baseline
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Baseline
|
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SNB
Tijdsspanne: Baseline
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Baseline
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ANB
Tijdsspanne: Baseline
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Baseline
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SN-GoGn
Tijdsspanne: Baseline
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Baseline
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L1-GoGn
Tijdsspanne: Baseline
|
Baseline
|
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U1-ANSPNS
Tijdsspanne: Baseline
|
Baseline
|
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Nasolabial angle
Tijdsspanne: Baseline
|
Baseline
|
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Facial angle
Tijdsspanne: Baseline
|
Baseline
|
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Wits appraisal
Tijdsspanne: Baseline
|
Baseline
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N-Me
Tijdsspanne: Baseline
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Baseline
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 juni 2026
Primaire voltooiing (Geschat)
30 september 2026
Studie voltooiing (Geschat)
30 september 2026
Studieregistratiedata
Eerst ingediend
17 juni 2026
Eerst ingediend dat voldeed aan de QC-criteria
17 juni 2026
Eerst geplaatst (Werkelijk)
24 juni 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
24 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
17 juni 2026
Laatst geverifieerd
1 juni 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- 2026-CEPHTRACING
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Beschrijving IPD-plan
Data will be available upon motivated request to the corresponding authors.
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .