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Not yet recruitingNCT07551622Updated Apr 27, 2026

Research on Deep Learning-Based Intelligent Diagnosis and Treatment

An observational study in Malocclusion, Craniofacial Morphology and Dentofacial Deformities, sponsored by Xi'an Jiaotong University. Not yet recruiting. Open to participants aged 6 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-27.

Sponsored by Xi'an Jiaotong University · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,000
Ages
6 Years to 70 Years
Sex
All
01

Study summary

This study aims to develop and evaluate deep learning-based artificial intelligence models for craniomaxillofacial multi-modal imaging analysis and clinical decision support. Approximately 2,000 participants with craniomaxillofacial imaging data and related clinical information will be included. The imaging data may include two-dimensional facial photographs, cone-beam computed tomography images, and three-dimensional facial surface scans.

The study will use artificial intelligence methods to analyze craniofacial images and identify clinically meaningful features related to facial morphology, skeletal or dental classification, anatomical landmarks, regional structures, and craniomaxillofacial abnormalities. The models will be developed for tasks such as image classification, anatomical landmark detection, image segmentation, abnormality recognition, and treatment-related decision support.

The purpose of this study is to improve the accuracy, efficiency, and consistency of image-based assessment in dentistry, orthodontics, and oral and maxillofacial clinical practice. The artificial intelligence models developed in this study are intended to provide objective imaging analysis and decision-support information for health care providers. These models are designed to assist clinicians and will not replace professional diagnosis or individualized treatment planning by qualified clinicians.

This research may benefit patients and families by supporting earlier and more accurate recognition of craniomaxillofacial conditions, improving communication about diagnosis and treatment options, and promoting more personalized oral health care. All clinical images and related information will be handled according to approved research procedures and privacy protection requirements.

Read the detailed description

This study is an imaging-based clinical artificial intelligence study that aims to develop, train, and validate deep learning models for craniomaxillofacial multi-modal imaging analysis and intelligent clinical decision support. Approximately 2,000 participants are planned to be enrolled. All participants will have craniomaxillofacial imaging data and related clinical information obtained during routine dental, orthodontic, oral and maxillofacial, or related clinical care.

The imaging data used in this study may include two-dimensional facial photographs, cone-beam computed tomography images, and three-dimensional facial surface scans. Related clinical data may include demographic information, clinical diagnosis, skeletal or dental classification, cephalometric measurements, treatment-related records, and available expert assessments. This study will focus on developing artificial intelligence models for craniomaxillofacial image classification, anatomical landmark detection, regional segmentation, abnormality recognition, and treatment-related decision support.

Before model development, all imaging data will undergo standardized preprocessing. Preprocessing procedures may include image de-identification, quality assessment, format conversion, image orientation correction, cropping, resolution standardization, grayscale or intensity normalization, spatial registration, and region-of-interest extraction. For two-dimensional images, standardized facial or radiographic regions will be defined according to the specific imaging task. For cone-beam computed tomography and three-dimensional facial surface data, preprocessing may include volumetric reconstruction, surface reconstruction, mesh processing, point-cloud processing, or anatomical structure extraction.

Reference labels will be derived from clinical medical records, clinician diagnosis, and expert manual annotation. For segmentation tasks, anatomical regions or structures will be manually annotated by trained clinicians or calibrated researchers. For landmark detection tasks, predefined anatomical landmarks will be annotated according to standardized craniomaxillofacial measurement protocols. For classification tasks, skeletal pattern, dental relationship, craniomaxillofacial morphology category, or other clinically meaningful classification labels will be determined based on expert assessment. Inter-observer and intra-observer consistency will also be evaluated to ensure the reliability of manual annotations and clinical labels.

The dataset of approximately 2,000 participants will be divided into training, validation, and testing datasets. Seventy percent of the data will be used for model training, 15% for model validation, and 15% for independent testing.

Deep learning models will include convolutional neural networks, attention-based models, and multi-task learning models. Model development will include hyperparameter optimization, regularization, data augmentation, and performance monitoring based on the validation dataset.

For image segmentation tasks, model performance will be evaluated using segmentation accuracy metrics, including the Dice similarity coefficient, Intersection over Union, pixel-wise accuracy, sensitivity, specificity, and, where applicable, boundary distance metrics such as Hausdorff distance or average surface distance. For image classification and diagnostic recognition tasks, model performance will be evaluated using accuracy, precision, recall, F1-score, sensitivity, specificity, positive predictive value, negative predictive value, receiver operating characteristic curve analysis, and area under the receiver operating characteristic curve. Confusion matrices will be used to describe the distribution of correct and incorrect classifications across diagnostic categories. For multi-class classification tasks, macro-averaged and weighted-averaged performance metrics may be reported. For anatomical landmark detection tasks, model performance will be evaluated using mean radial error, mean absolute error, successful detection rate within clinically meaningful distance thresholds, and agreement with expert annotations.

For treatment-related decision support tasks, model outputs will be compared with expert clinical judgment. Evaluation metrics will include accuracy, precision, recall, F1-score, AUC, and decision curve analysis.

Personnel involved in image annotation and data processing will receive relevant training before the start of the study. Access to identifiable personal information will be restricted to authorized research personnel. The analysis datasets used for model development will be de-identified or pseudonymized whenever possible.

The planned enrollment of approximately 2,000 participants is expected to support subgroup analyses and robustness testing when the distribution of imaging modalities and clinical categories is adequate. Missing, unavailable, uninterpretable, or inconsistent data will be recorded.

The artificial intelligence models developed in this study are intended to assist health care providers in craniomaxillofacial imaging analysis and clinical decision support. The models will not replace professional clinical diagnosis or individualized treatment planning by qualified clinicians. Any future clinical application of these models will require further validation, clinical review, and appropriate institutional or regulatory approval.

02

Conditions studied

  • Malocclusion
  • Craniofacial Morphology
  • Dentofacial Deformities
03

In context

Malocclusion

323 studies on the registry are indexed under Malocclusion; 85 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 63 across 74 observational studies indexed under Malocclusion.

Browse Malocclusion studies →

Lead sponsor

Xi'an Jiaotong University is the lead sponsor of 32 studies on the registry; 8 are open to participants now.

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

04

Who can participate

Ages eligible
6 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will include approximately 2,000 participants with craniomaxillofacial imaging data and related clinical information obtained during routine dental, orthodontic, oral and maxillofacial, or related clinical care. Eligible participants may have two-dimensional facial photographs, cone-beam computed tomography images, or three-dimensional facial surface scans available for artificial intelligence-based imaging analysis. Related clinical information may include demographic characteristics, clinical diagnosis, skeletal or dental classification, cephalometric measurements, treatment-related records, and expert assessment results. The study will use available clinical imaging data to develop and validate deep learning models for craniomaxillofacial image classification, segmentation, landmark detection, abnormality recognition, and treatment-related decision support.

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

  • Participants with available craniomaxillofacial imaging data obtained during routine dental, orthodontic, oral and maxillofacial, or related clinical care.
  • Participants with at least one eligible imaging modality, including two-dimensional facial photographs, cone-beam computed tomography images, or three-dimensional facial surface scans.
  • Participants with related clinical information available for model development or validation, such as demographic information, clinical diagnosis, skeletal or dental classification, cephalometric measurements, treatment-related records, or expert assessment results.
  • Imaging data of sufficient quality for artificial intelligence-based image analysis, annotation, segmentation, landmark detection, classification, or decision-support model development.

Exclusion criteria

Exclusion Criteria:

  • Participants with incomplete or unavailable key imaging data or clinical information required for the planned analysis.
  • Images with severe artifacts, poor resolution, incorrect orientation, incomplete anatomical coverage, or other quality problems that prevent reliable analysis.
  • Duplicate records or repeated imaging records that cannot be reliably linked to a unique participant.
  • Participants whose data cannot be used according to institutional review board approval, consent requirements, or applicable privacy protection regulations.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Craniomaxillofacial Imaging Cohort

    Participants with available craniomaxillofacial imaging data and related clinical information obtained during routine dental, orthodontic, oral and maxillofacial clinical care.

06

What researchers measure

Primary outcomes

  1. Diagnostic performance of artificial intelligence models for craniomaxillofacial imaging analysis

    The primary outcome is the diagnostic performance of the developed artificial intelligence models on the independent testing dataset. Performance will be evaluated using accuracy, precision, recall, F1-score, sensitivity, specificity, positive predictive value, negative predictive value, receiver operating characteristic curve analysis, and area under the receiver operating characteristic curve, as appropriate for the specific classification or diagnostic recognition task.

    Time frame: At completion of model validation on the independent testing dataset, expected within 12 months after study initiation

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for May 2026; primary completion for Dec 2027, 19 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 19, 2026
First posted
Apr 27, 2026
StartEst.
May 1, 2026
Primary completionEst.
Dec 31, 2027
CompletionEst.
Dec 31, 2029
Last update
Apr 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07551622
Lead sponsor
Xi'an Jiaotong University
Responsible party
Yuxin Guo (Research Assistant Professor, Xi'an Jiaotong University) — Principal investigator
First posted
Apr 27, 2026
Start date
May 1, 2026 (estimated)
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Apr 27, 2026

Study contacts

Yu xin Guo, Ph.D
Contact
guoyuxin@xjtu.edu.cn
+86 17782626326
Hui Yang, master candidate
Contact
yanghui1585981@163.com
+86 15859811830

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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