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Clinical Evaluation of AI-Generated Dental Crowns

2026年4月24日 更新者:The University of Hong Kong

A Clinical Research in Using Artificial Intelligence (AI) to Design Dental Crown

This clinical research validates a fully automatic AI algorithm for dental crown design using GANs trained on University of Hong Kong 3D prosthesis data and AI-powered FEA for stress correction, overcoming CAD/CAM limitations like manual technician time and occlusal errors. In-vitro fatigue tests confirmed performance comparable to conventional crowns. Clinically, AI-designed crowns are compared to technician CAD/CAM controls using 10 FDI criteria (aesthetic/functional/biological), assessed via oral exams, and IOS (wear), to prove feasibility and optimize the algorithm.

研究概览

详细说明

Artificial Intelligence (AI) is the science and engineering of machines that act intelligently (1). The Oxford Dictionary defines AI as the theory and development of computer systems able to perform tasks normally requiring human intelligence, such as visual perception, speech recognition, decision making, and translation between languages (2). There are many ways AI can be achieved, the most important among them are 1) Machine learning: It is a method where the target is defined and the steps to reach that target is learned by the machine itself by training (gaining experience); 2) Natural language processing, for example, Siri and Google assistant. 3) Computer vision, for example, tesla Autopilot. Many fields have already benefited from AI. In medical field, AI has already been implemented in various medical fields in diagnosis such as diabetic retinopathy, skin cancer and breast lesions (3). In dentistry, most of the application goes to the automatic diagnosis based on CT and radiology images (4).

Digital workflow has become an overwhelming trend in dentistry motivated by the prevalence of intraoral scanners (IOS) and computer aided design and computer aided manufacturing (CAD/CAM). Compared with traditional laboratory methods, which are regarded as time-consuming and technically sensitive, the digital workflow can be greatly convenient and efficient (5). Thus, CAD/CAM facilitates the opportunity for improving the productivity of dental prosthesis.

Current digital workflow consists of four basic elements: 1) tooth preparation and data acquisition (via intraoral scanner, x-ray, CBCT, etc.), 2) data processing and prosthesis design (via CAD), 3) prosthesis fabrication (either laboratory or chairside milling via CAM), and 4) try-in and cementation in the clinic (by the dentist). Despite all the advancements such as the elimination of physical models and labour-saving, many problems still exist in the current workflow. Each dental prosthesis must be customized to meet individual patients' condition and requirement. Designing dental restoration must be conducted and approved by the technician; this is a time-consuming and labour-intensive process even with the assistance of CAD software. In particular, the wrong design in CAD process makes the crowns that can induce major oral problems of: 1) Superocclusion, 2) Infraocclusion, and 3) Overcontour. This said, CAD/CAM does not save a lot of the dentists' and patients' time and cost as advocated. Therefore, there is a need to change the current practice of dental CAD/CAM.

In view of this, with the support of GRF, we have developed a fully automatic algorithm for the design of dental prosthesis by utilizing AI technology. The algorithm was based on two aspects: 1) utilization of the current dental knowledge by learning the materials-human interactions and materials-biomaterials properties to automate the prosthetic design; 2) based on the previous clinically relevant studies, to validate the design from finite element analysis (FEA) results. With the 3D digital dental prosthesis dataset obtained from Prince Philip Dental Hospital, Faculty of Dentistry, The University of Hong Kong, Generative Adversarial Network (GAN) was adopted to train the machine learning model on the design of dental prosthesis. It composed of two deep networks, the generator, and the discriminator. The discriminator could identify the tiny difference between the real and the generated designs, and the generator could create the designs that discriminator cannot tell the difference. Finally, the GAN model converges and produces natural look designs of prosthesis. Afterwards, an AI-enabled FEA algorithm was established in order to achieve the accurate and fast FEA of dental prosthesis. Stress concentration on the prepared tooth and prosthesis, a common cause of the failure, may result from flawed prosthesis design. Based on our published FEA data (6, 7), a validation model was built mainly to detect and correct the errors of design which may cause stress concentration. This FEA machine learning model also served as one of the criteria on evaluating the quality of automatic generated prosthesis.

After the training via GAN and machine learning model, the automatic prosthesis design algorithm needs to be validated by means of mechanical tests in the laboratory and application in clinical practice. Cyclic fatigue is prone to cause failure from stress concentration areas or loading contact points; however, it is hard to be detected by technicians directly (8, 9). In in-vitro validation, specimens were subject to cyclic loading using the Instron universal testing machine (Electro Puls E3000, Instron, Norwood, USA), then failure mode analysis and scanning electron microscopy (SEM) were conducted. Comparable fatigue properties of the automatically designed prosthesis to that of CAD/CAM prosthesis have been confirmed (7, 10).

Therefore, several clinically relevant parameters, such as anatomical form, marginal adaptation, wear behaviour of the restoration and the antagonist, and integrity of the restoration and the abutment tooth, are aimed to be evaluated clinically using World Dental Federation (FDI) criteria (11). Compared with the modified USPHS criteria, FDI criteria may give more sensitive results in relatively short-term clinical trials, as it has more scoping options (12). The criteria can be categorized into aesthetic parameters (4 items), functional parameters (6 items) and biological parameters (6 items). In this study, 10 items are selected as they are relevant to the design procedure of the prosthesis. Data collection will be accomplished using oral examination and grading and IOS.

In evaluation of the amount of wear, digital impressions captured by IOS can be superimposed and analysed directly in the software. The replica is no longer needed, the data capture procedure is simplified, so the error can be reduced. IOS has been utilized in several clinical assessments and its accuracy has been confirmed (15).

This proposal aims at validating prosthesis design by the fully automatic algorithm both clinical side and also to further optimize the algorithm. Restorations designed by the algorithm will be comprehensively evaluated according to the FDI criteria while the CAD/CAM prostheses designed by technicians using ordinary computer-aided design software serve as the control group.

Reference:

  1. Norvig P. Artificial intelligence: Early ambitions. New Scientist. 2012;216(2889):ii-iii.
  2. OxfordUniversityPress. English Oxford Dictionaries. Oxford University Press; 2019.
  3. He J, Baxter SL, Xu J, Xu J, Zhou X, Zhang K. The practical implementation of artificial intelligence technologies in medicine. Nature medicine. 2019;25(1):30.
  4. Hwang J-J, Jung Y-H, Cho B-H, Heo M-S. An overview of deep learning in the field of dentistry. 2019.
  5. Li RW, Chow TW, Matinlinna JP. Ceramic dental biomaterials and CAD/CAM technology: state of the art. J Prosthodont Res. 2014;58(4):208-16.
  6. Maghami E, Homaei E, Farhangdoost K, Pow EHN, Matinlinna JP, Tsoi JK-H. Effect of preparation design for all-ceramic restoration on maxillary premolar: a 3D finite element study. Journal of prosthodontic research. 2018;62(4):436-42.
  7. Homaei E, Jin X-Z, Pow EHN, Matinlinna JP, Tsoi JK-H, Farhangdoost K. Numerical fatigue analysis of premolars restored by CAD/CAM ceramic crowns. Dental Materials. 2018;34(7):e149-e57.
  8. Keulemans F, Palav P, Aboushelib MM, van Dalen A, Kleverlaan CJ, Feilzer AJ. Fracture strength and fatigue resistance of dental resin-based composites. Dent Mater. 2009;25(11):1433-41.
  9. Zhang Z, Guazzato M, Sornsuwan T, Scherrer SS, Rungsiyakull C, Li W, et al. Thermally induced fracture for core-veneered dental ceramic structures. Acta Biomater. 2013;9(9):8394-402.
  10. Homaei E, Pow EHN, Matinlinna JP, Akbari M, Tsoi JK-H. Fatigue resistance of monolithic CAD/CAM ceramic crowns on human premolars. Ceramics International. 2016;42(14):15709-17.
  11. Hickel R, Peschke A, Tyas M, Mjor I, Bayne S, Peters M, et al. FDI World Dental Federation: clinical criteria for the evaluation of direct and indirect restorations-update and clinical examples. Clin Oral Investig. 2010;14(4):349-66.
  12. Cakir NN, Demirbuga S. The effect of five different universal adhesives on the clinical success of class I restorations: 24-month clinical follow-up. Clin Oral Investig. 2019;23(6):2767-76.
  13. Sinescu C, Negrutiu M, Topala F, Ionita C, Negru R, Fabriky M, et al. Ceramic and Polymeric Dental Onlays Evaluated by Photo elasticity, Optical Coherence Tomography and Micro Computed Tomography. Proc Spie. 2011;8172.
  14. Fujita R, Komada W, Nozaki K, Miura H. Measurement of the remaining dentin thickness using optical coherence tomography for crown preparation. Dent Mater J. 2014;33(3):355-62.
  15. Aladag A, Oguz D, Comlekoglu ME, Akan E. In vivo wear determination of novel CAD/CAM ceramic crowns by using 3D alignment. J Adv Prosthodont. 2019;11(2):120-7.

研究类型

介入性

注册 (实际的)

40

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Hong Kong、香港、000000
        • Faculty of Dentisry, the University of Hong Kong

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Both male and female patients (aged 18-60 years old) attending the HKU Faculty of Dentistry teaching clinic in Prince Philip Dental Hospital (PPDH), who are in need of single crown restorative treatment in the posterior region.

Exclusion Criteria:

  • female patients with pregnancy; patients with any systemic diseases (e.g., uncontrolled diabetes, uncontrolled hypertension, uncontrolled osteoporosis, etc); patients with history of local irradiation therapy; patients with untreated periodontal diseases or poor oral hygiene; patients with severe bruxism or clenching habits; patients with periapical lesions in the treated teeth.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:AI-designed crowns
Participants receive single-unit dental crowns automatically designed by a fully AI-based algorithm using Generative Adversarial Networks (GAN) trained on 3D clinical prosthesis data from the University of Hong Kong.
Single-unit dental crowns automatically designed by a fully AI-based algorithm using Generative Adversarial Networks (GAN) trained on 3D dental prosthesis datasets from the University of Hong Kong.
有源比较器:Conventional CAD/CAM Dental Crowns
Participants receive single-unit dental crowns designed manually by experienced dental technicians using standard computer-aided design and computer-aided manufacturing (CAD/CAM) software and workflow (current standard of care).
Single-unit dental crowns designed manually by experienced dental technicians using standard CAD software and fabricated using computer-aided manufacturing (CAM) methods (milling or 3D printing). This represents the current standard-of-care digital workflow for dental restorations.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Fracture of material or tooth and loss of retention
大体时间:12 months (baseline + 6, 12months post-cementation)
Primary outcome variables are the fracture of material or tooth and loss of retention. These major failures (graded as "Clinically poor - replacement necessary" on FDI criteria) are assessed by oral examination and IOS for detection of fractures, cracks, or debonding.
12 months (baseline + 6, 12months post-cementation)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2022年9月5日

初级完成 (实际的)

2025年12月7日

研究完成 (估计的)

2027年1月31日

研究注册日期

首次提交

2026年4月24日

首先提交符合 QC 标准的

2026年4月24日

首次发布 (实际的)

2026年5月1日

研究记录更新

最后更新发布 (实际的)

2026年5月1日

上次提交的符合 QC 标准的更新

2026年4月24日

最后验证

2026年3月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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