Dental Occlusion

6

Review clinical trials related to Dental Occlusion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Occlusal Changes After Modified Hall Technique in Molars Affected by Molar-Incisor Hypomineralization

Molar-incisor hypomineralization (MIH) frequently affects permanent first molars and increases the risk of rapid post-eruptive breakdown and restorative failure. Stainless steel crowns (SSCs) are considered a reliable treatment option for severely affected molars; however, SSC placement may temporarily alter the occlusal vertical dimension and occlusal contacts. Quantitative evidence describing the occlusal adaptation process following SSC placement in MIH-affected permanent molars is limited. This prospective longitudinal clinical study aims to evaluate occlusal adaptation after SSC placement using the modified Hall technique in MIH-affected permanent first molars. Forty-six children will be included. Intraoral scans will be obtained at baseline, immediately after treatment, and during follow-up visits up to 3 months. Digital models will be superimposed to measure three-dimensional changes in cusp position, occluso-vertical dimension, and occlusal contact area. Temporomandibular joint function and periodontal parameters will also be assessed. The results are expected to provide quantitative evidence on occlusal adaptation following SSC treatment in MIH-affected molars.

Participants needed: 46
Trial details
Age: 6-14Biological sex: AllType: InterventionalSponsor: Ankara Yildirim Beyazıt UniversityUpdated: Apr 17, 2026Locations: 1
Eligibility criteria

Absence of any skeletal anomalies [+11]

Individuals with serious systemic or psychological conditions [+2]

Status: Not yet recruiting

Evaluation of Occlusal Adjustment Material Removal on Monolithic Zirconia Blocks: An In Vitro Study

This study aims to improve understanding of the amount of tooth-replacement material removed during a single grinding "stroke" performed in the adjustment of a zirconia crown. Zirconia is a highly durable ceramic material commonly used for dental restorations, and accurate adjustment is essential for achieving proper occlusion. However, existing literature does not provide quantitative data regarding material removal per stroke during chairside adjustment, resulting in reliance on individual clinical experience. In this study, standardized zirconia specimens will be prepared and assigned to three operator groups: dental students, dental interns, and experienced clinicians. Each participant will perform a controlled number of grinding strokes on the specimens using a commonly used dental grinding stone. Specimens will be scanned before and after grinding using a three-dimensional scanner to precisely quantify material removal. Hypothesis The hypotheses of this study are: Each grinding stroke results in a measurable and relatively consistent amount of zirconia material removal. Experienced clinicians demonstrate more controlled and predictable material removal per stroke compared with students and interns.

Participants needed: 120
Trial details
Age: 20-40Biological sex: AllType: ObservationalSponsor: National Taiwan University HospitalUpdated: Dec 30, 2025
Eligibility criteria

Acute upper-limb/hand injuries or postoperative recovery within the past 3 month... [+3]

Status: Not yet recruiting

Digital Occlusal Analysis and Bite Force Evaluation of Primary Molars Restored With Zirconia Crowns Using T-Scan

The goal of this observational study is to evaluate the adaptation of occlusion and bite force after zirconia crown restoration in children with pulp-treated primary molars. The main questions it aims to answer are: How does occlusion adapt after placement of zirconia crowns? Does bite force change following crown restoration? Participants will: Undergo routine pulp treatment and restoration of primary molars with zirconia crowns. Have bite force and occlusal contacts measured using the T-Scan digital occlusal analysis system before and after crown placement.

Participants needed: 11
Trial details
Age: 6-9Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

Children aged 6 to 9 years. [+7]

Children with medical conditions or who are uncooperative during dental care. [+6]

Status: Recruiting

Occlusal Impact of Hall Crowns in Primary Molars

Hall Technique is a non-invasive restorative approach for managing carious primary molars, increasingly used in pediatric dentistry due to its simplicity and patient tolerance. This study aims to evaluate and compare the occlusal changes that occur following Hall crown placement on different primary molar groups (maxillary first molar, maxillary second molar, mandibular first molar, mandibular second molar) using digital model analysis.

Participants needed: 60
Trial details
Age: 7-10Biological sex: AllType: InterventionalSponsor: Ankara Yildirim Beyazıt UniversityUpdated: Nov 20, 2025Locations: 1
Eligibility criteria

No skeletal or dental anomalies, [+19]

Individuals with serious systemic or psychological conditions [+2]

Status: Not yet recruiting

Digital vs Conventional Prosthetic Rehab & Occlusal Analysis in Edentulous Patients

15 Patients requiring complete dentures will be recruited from Dubai Health. Each patient will receive two sets of dentures with a washout period between sets. Patients will remain blinded to the fabrication method used for each set. * Group 1: Participants will first receive conventionally fabricated dentures for both the upper and lower jaws. This set will be made using traditional techniques, including impressions, a custom tray, jaw relation recording, try-in, and final fitting. After the washout period, they will receive a second set created with the 3D-printed technique. * Group 2: Participants in this group will initially receive 3D-printed complete dentures through a digital workflow, which involves intraoral scanning, STL file export, digital design, design review with the patient, 3D printing, and final fitting. Following the washout period, they will then receive a conventionally fabricated set.

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mohammed Bin Rashid University of Medicine and Health SciencesUpdated: Sep 9, 2025
Eligibility criteria

Adults above the age of eighteen years seeking replacement of missing teeth [+2]

Temporomandibular Joint Disorders(TMD) [+3]

Status: Recruiting

Patient Perception and Oral Function of Implant Restorations

The overall aim is to evaluate the patient-reported outcome and efficiency of replacing posterior teeth with implant-supported crowns compared to RDPs and no treatment. Sub-aims are to evaluate a new 3D-methods for registration of occlusion and to test two crown designs. Thus, the study design has three aims: * To analyze patient perception including OHRQoL, when missing posterior teeth are replaced with implant-supported crowns compared to removable dental prostheses (RDPs) or no replacement. * To develop and validate new 3D digital methods for assessing occlusal contacts between upper and lower jaw and to analyze the methods relation to masticatory ability and efficiency. * To compare the difference in biological technical outcomes between splinted and non-splinted implant-supported crowns over time.

Participants needed: 20
Trial details
Age: 30+Biological sex: AllType: InterventionalSponsor: University of CopenhagenUpdated: Jul 5, 2024Locations: 1
Eligibility criteria

Partially edentulous subjects with missing posterior teeth (Kennedy class I or c...

Untreated or active, progressive periodontitis [+11]