← Back to all trials
Completed
NCT07834957
Clinical Evaluation of AI-Driven Designed Single Crowns
Conditions: Artificial Intelligence in Dental Crown Design, Tooth Crown Restoration, Dental Restorations
Sex: All
Ages: 20 Years – 39 Years
Healthy volunteers: No
Phase: NA
Enrollment: 47
Sponsor: Hacettepe University
Location: Hacettepe University Faculty of Dentistry, Department of Prosthodontics Ankara Ankara
Summary
This clinical study compares tooth-supported single crowns designed by a dental technician and by an artificial intelligence (AI) driven automated design method. The two design methods are qualitatively compared in terms of buccal and lingual/palatal contours, proximal and occlusal contacts, and marginal fit using clinical evaluation. The two design methods are quantitatively compared in terms of global, buccal, and lingual/palatal surface deviations using three-dimensional surface deviation analysis.
Eligibility Criteria
Inclusion Criteria:
* Provision of written informed consent to participate in the study
* Adults aged 20-39 years
* Good general and local periodontal health with adequate oral hygiene
* Indication for a single full-coverage crown restoration in the posterior region
* Asymptomatic abutment tooth on clinical examination
* No periradicular radiolucency associated with the abutment tooth on periapical radiographic examination
* Sufficient remaining tooth structure without the need for a post-and-core restoration, allowing preservation of at least three axial walls after preparation, achievement of a ferrule with at least 1 mm of sound tooth structure coronal to the gingival level, and standardized finish-line preparation
* Presence of intact natural teeth or restorations mesial and distal to the abutment tooth and an opposing tooth or restoration allowing establishment of occlusal contact
* Stable interarch occlusal relationship
* No parafunctional habits
Exclusion Criteria:
* Refusal to provide written informed consent
* Serious systemic disease or condition that may contraindicate or interfere with tooth preparation and restorative treatment, including steroid therapy, uncontrolled diabetes mellitus, immunological disorders, pregnancy, or conditions preventing adequate cooperation
* Systemic or local risk factors that may affect the treatment process, including active periodontal disease or inadequate oral hygiene
* History of allergy to local anesthetics containing epinephrine
* Functional or muscular temporomandibular disorders limiting mouth opening
* Parafunctional habits such as bruxism
Source: ClinicalTrials.gov (NCT07834957). StuddyBuddy aggregates publicly available trial information.