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RecruitingNCT07664488Updated Jun 24, 2026

Comparison of Digital Analysis and Artificial Intelligence for Cephalometric Tracing

An observational study in Cephalometric Analysis, Cephalometry and Artificial Intelligence (AI), sponsored by University of Pavia. Recruiting at 1 site in Italy. Per ClinicalTrials.gov, last updated 2026-06-24.

Sponsored by University of Pavia · Observational

From the registry’s dates

  • Started Jun 2026; still recruiting 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Sex
All
01

Study summary

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.

Read the detailed description

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.

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Conditions studied

  • Cephalometric Analysis
  • Cephalometry
  • Artificial Intelligence (AI)
  • Artificial Intelligence (AI) in Diagnosis

Keywords

  • artificial intelligence
  • cephalometric analysis
  • lateral cephalogram
  • landmark identification
  • automated cephalometric tracing
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In context

Lead sponsor

University of Pavia is the lead sponsor of 144 studies on the registry; 39 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

    Diagnostic Test: Cephalometric Analysis

Interventions

  • Diagnostic testCephalometric Analysis

    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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What researchers measure

Primary outcomes

  1. Agreement between AI-based cephalometric analysis and digital manual tracing

    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.

    Time frame: Baseline

Secondary outcomes

  1. SNA

    Time frame: Baseline

  2. SNB

    Time frame: Baseline

  3. ANB

    Time frame: Baseline

  4. SN-GoGn

    Time frame: Baseline

  5. L1-GoGn

    Time frame: Baseline

  6. U1-ANSPNS

    Time frame: Baseline

  7. Nasolabial angle

    Time frame: Baseline

  8. Facial angle

    Time frame: Baseline

  9. Wits appraisal

    Time frame: Baseline

  10. N-Me

    Time frame: Baseline

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Study locations

1 of 1 sites recruiting
  • Unit of Orthodontics and Pediatric Dentistry - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Pediatrics - University of Pavia, Pavia, Lombardy 27100
    Pavia, Italy 27100, Italy
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — Data will be available upon motivated request to the corresponding authors.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07664488
Responsible party
Andrea Scribante (Prof., University of Pavia) — Principal investigator
First posted
Jun 24, 2026
Start date
Jun 1, 2026
Primary completion
Sep 30, 2026 (estimated)
Completion
Sep 30, 2026 (estimated)
Last update
Jun 24, 2026

Study contacts

Andrea Scribante, DDS, PhD
Contact
andrea.scribante@unipv.it
+39 0382516223

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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