Evaluation of Temporomandibular Disorders and Their Association With Tooth Wear Using Digital Methods
Evaluation of the Prevalence of Temporomandibular Disorders and Lts Association With Tooth Wear Measured Using Digital Methods
1 other identifier
observational
120
1 country
1
Brief Summary
Temporomandibular disorders (TMDs) are considered complex conditions in dental practice due to their multifactorial etiology. Over the years, various diagnostic methods have been introduced; however, the most widely accepted model to explain the complexity of TMD is the biopsychosocial model. The Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) Axis I and Axis II protocol is currently regarded as the gold standard for evaluating TMDs. Today, studies employing the DC/TMD framework are conducted in various populations. This study aims to assess the prevalence of TMD using updated diagnostic criteria. In addition, it seeks to evaluate the presence of tooth wear-one of the common clinical findings associated with TMD-through digital measurement and visual assessment tools, and to investigate its correlation with TMD. Specifically, the study will examine how changes in occlusal contact points due to bruxism and wear are reflected in functional changes within the temporomandibular joint (TMJ) and the extent of tooth wear. The effects of both mild and severe tooth wear on TMJ health and their potential long-term implications for oral health will also be explored. The primary objective of this study is to determine the prevalence of TMD in the general population using the DC/TMD Axis I and Axis II protocols and to evaluate the impact of tooth wear-measured via digital intraoral scanners-on TMD. Special attention will be given to how changes in occlusal contact due to bruxism and wear influence stress distribution and adaptive remodeling in TMJ structures. Furthermore, the study aims to compare the effects of mild versus severe tooth wear on joint function, ultimately contributing to the development of early diagnosis and intervention strategies. Additionally, this study seeks to highlight the effectiveness of digital technologies, such as intraoral scanners and 3D modeling, in evaluating the relationship between tooth wear and TMJ disorders. By doing so, the research aims to enhance the existing literature on the link between tooth wear and TMD and provide evidence-based guidance for clinical practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Dec 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 26, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 30, 2025
CompletedFirst Submitted
Initial submission to the registry
July 5, 2025
CompletedFirst Posted
Study publicly available on registry
July 23, 2025
CompletedJuly 23, 2025
July 1, 2025
2 months
July 5, 2025
July 15, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Occlusal contact area percentage in posterior teeth (%)
Occlusal contact area will be calculated as a percentage of the total occlusal surface area in posterior teeth. Digital impressions will be acquired using the Medit i700 intraoral scanner. Contact points will be identified with the Medit Occlusal Analyzer plugin, and contact areas will be measured from STL files using ImageJ software (version 1.54). The percentage will be computed by dividing the total occlusal contact area by the total occlusal surface area.
Baseline (Day 1 of clinical evaluation)
Secondary Outcomes (2)
Tooth wear severity score assessed by TWES 2.0 (ordinal scale: 0-4)
Baseline (Day 1 of clinical evaluation)
Pain severity score using Graded Chronic Pain Scale v2.0 (unit: 0-4 categorical score)
Baseline (Day 1 of clinical evaluation)
Eligibility Criteria
This study includes individuals aged 18 years and older who have an adequate number of premolar and molar teeth in the posterior region, without systemic diseases, and without active dental pain or recent trauma to the face or neck. All participants were voluntarily selected from among patients who applied to the Department of Prosthodontics at the Faculty of Dentistry, Necmettin Erbakan University.
You may qualify if:
- Adults aged 18 years and above
- Voluntary participation with signed informed consent
- Presence of a sufficient number of posterior teeth (premolars and molars)
- Willingness to undergo intraoral digital scanning
- Willingness to participate in occlusal contact analysis procedures
You may not qualify if:
- Presence of systemic diseases affecting the temporomandibular joint (TMJ)
- Active dental pain at the time of evaluation
- Recent trauma to the facial or jaw region
- Current psychiatric or neurological disorders
- History of orthodontic treatment or extensive prosthetic rehabilitation
- Pathological jaw dysfunctions not related to parafunctional activity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Necmettin Erbakan University
Konya, Konya, 42090, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- DDS
Study Record Dates
First Submitted
July 5, 2025
First Posted
July 23, 2025
Study Start
December 26, 2024
Primary Completion
February 20, 2025
Study Completion
May 30, 2025
Last Updated
July 23, 2025
Record last verified: 2025-07