- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05056948
Artificial Intelligence Designed Single Tooth Dental Prostheses
Artificial Intelligence in Prosthodontics - Design of Maxillary Single-tooth Dental Prostheses
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objectives:
- To compare four deep-learning methods/algorithms in interpreting and learning of the features of 3D models;
- To compare the AI system with maxillary tooth model alone to maxillary and mandibular (antagonist) models;
- To compare the occlusal morphology and 3D position of the single-tooth dental prostheses designed by trained AI and by dental technicians.
Methods:
First, investigators will collect 200 maxillary dentate teeth models as training models. AI will learn the relationship between individual teeth and rest of the dentition using the 3D Generative Adversarial Network (GAN) by following deep-learning methods/algorithms:
Group 1) Voxel-based; Group 2) View-based; Group 3) Point-based; and Group 4) Fusion methods. Investigators will collect another 100 maxillary models that serve as validation models. Investigators will remove a tooth (act as control) in each model. Then investigators will evaluate these deep learning algorithms in predicting the occlusal morphology and 3D position of single-missing tooth.
Second, investigators will evaluate the need of antagonist model in predicting the occlusal morphology and 3D position of single-missing tooth in 100 validation models:
Group i) maxillary model only and Group ii) with antagonist model using the tested deep-learning algorithm in objective (1).
Third, investigators will analyze the geometric morphometric and 3D position of dental prostheses designed by:
Group a) the trained AI system; Group b) dental technicians on the physical models; and Group c) dental technicians using CAD software. Investigators will compare these teeth to the corresponding natural teeth (control) in 100 validation models.
Furthermore, investigators will analyze the time required for tooth design in these groups as secondary outcome.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Sai Ying Pun, Hong Kong
- Prince Philip Dental Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
- Patients attended/attending Prince Philip Dental Hospital
- Dental undergraduate students from the Faculty of Dentistry, The University of Hong Kong
Description
Inclusion Criteria:
- Subjects with sufficient dentition present for the determination of the upper occlusal plane
- Subjects with more than 12 occluding pairs and stable intercuspal position
- Subjects with teeth restorations that did not grossly alter its morphology
- Subjects who did not undergo orthodontic treatment and/or did not have teeth that rotated more than 45 degrees and/or displaced more than 1.5 mm
- Subjects who are of Cantonese descent.
Exclusion Criteria:
- Subjects with periodontal disease whereby there is pathological tooth migration and alteration of occlusal plane.
- Subjects who are under the age of 18 and unable to give consent.
- Subjects with extensive teeth restorations that affect the morphology.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Control
Original 3D maxillary teeth model from subjects who fulfill inclusion/exclusion criteria
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Test
3D maxillary teeth model from subjects who fulfill inclusion/exclusion criteria. The right first molar (FDI number 16) will be removed in the computer and then designed by artificial intelligence (AI) system AI system will be trained by
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Maxillary right first molar will be removed in the computer and will be designed by artificial intelligence system
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
3D position of tooth
Time Frame: Outcome will be measured when 25% of training models were studied by AI, up to 6 months
|
The center of a tooth automatically determined by computer
|
Outcome will be measured when 25% of training models were studied by AI, up to 6 months
|
|
3D position of tooth
Time Frame: Outcome will be measured when 50% of training models were studied by AI, up to 12 months
|
The center of a tooth automatically determined by computer
|
Outcome will be measured when 50% of training models were studied by AI, up to 12 months
|
|
3D position of tooth
Time Frame: Outcome will be measured when 75% of training models were studied by AI, up to 18 months
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The center of a tooth automatically determined by computer
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Outcome will be measured when 75% of training models were studied by AI, up to 18 months
|
|
3D position of tooth
Time Frame: Outcome will be measured after the whole training, which AI was trained of 100% of all models, up to 24 months
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The center of a tooth automatically determined by computer
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Outcome will be measured after the whole training, which AI was trained of 100% of all models, up to 24 months
|
|
Occlusal morphology of tooth
Time Frame: Outcome will be measured when 25% of training models were studied by AI, up to 6 months
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The cusps (highest point) and the fossa (lowest point) of the occlusal surface
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Outcome will be measured when 25% of training models were studied by AI, up to 6 months
|
|
Occlusal morphology of tooth
Time Frame: Outcome will be measured when 50% of training models were studied by AI, up to 12 months
|
The cusps (highest point) and the fossa (lowest point) of the occlusal surface
|
Outcome will be measured when 50% of training models were studied by AI, up to 12 months
|
|
Occlusal morphology of tooth
Time Frame: Outcome will be measured when 75% of training models were studied by AI, upto 18 months
|
The cusps (highest point) and the fossa (lowest point) of the occlusal surface
|
Outcome will be measured when 75% of training models were studied by AI, upto 18 months
|
|
Occlusal morphology of tooth
Time Frame: Outcome will be measured after the whole training, which AI was trained of 100% of all models, upto 24 months
|
The cusps (highest point) and the fossa (lowest point) of the occlusal surface
|
Outcome will be measured after the whole training, which AI was trained of 100% of all models, upto 24 months
|
|
Time spent in laboratory design and in clinical deliver of denture prostheses
Time Frame: Outcome will be measured after the whole training, which AI was trained of 100% of all models, upto 24 months
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Time (in minutes) spend in a) design and b) deliver of dental prostheses
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Outcome will be measured after the whole training, which AI was trained of 100% of all models, upto 24 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Walter Lam, BDS, MDS, The University of Hong Kong
Publications and helpful links
General Publications
- Chow TW, Clark RK, Cooke MS. The orientation of the occlusal plane in Cantonese patients. J Dent. 1986 Dec;14(6):262-5. doi: 10.1016/0300-5712(86)90034-5. No abstract available.
- Chow TW, Clark RK, Cooke MS. Errors in mounting maxillary casts using face-bow records as a result of an anatomical variation. J Dent. 1985 Dec;13(4):277-82. doi: 10.1016/0300-5712(85)90021-1. No abstract available.
- Lam WY, Hsung RT, Choi WW, Luk HW, Pow EH. A 2-part facebow for CAD-CAM dentistry. J Prosthet Dent. 2016 Dec;116(6):843-847. doi: 10.1016/j.prosdent.2016.05.013. Epub 2016 Jul 28.
- Lam WYH, Hsung RTC, Choi WWS, Luk HWK, Cheng LYY, Pow EHN. A clinical technique for virtual articulator mounting with natural head position by using calibrated stereophotogrammetry. J Prosthet Dent. 2018 Jun;119(6):902-908. doi: 10.1016/j.prosdent.2017.07.026. Epub 2017 Sep 29.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UW 20-848
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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