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Completed

NCT Number: NCT07366385

OccluSense is Sensor Based System Used as a Digital Method for Occlusal Contact Analysis, and Basically Used Without Any Support of Its Sensor. Therefore the Aim of This Study is to Clinically Evaluate the Validity of a Customizable Stabilizing Tray to Support OccluSense Sensor in.

Background: Occlusal contacts analysis is of prime importance in order to perform an effective prosthetic restoration. Quantitative methods for occlusal contact analysis involve using digital systems to measure and analyze occlusal contacts and forces with greater precision than traditional methods. One of these devices is the OccluSense which is sensor based system and basically used without any support of its sensor. Therefore the aim of this study is to clinically evaluate the validity of a customizable stabilizing tray to support the sensor of the OccluSense intraoral. A total of 22 healthy dental students, aged from 18-25 years, are recruited. Each participant will undergo two set of recordings; firstly by the OccluSense without centering tray then with the tray seated intraoral. Occlusal contacts were recorded under maximum bite force and Maximum Intercuspation Position (MIP).

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Key information

Conditions

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

faculty of dentistry Cairo University

Cairo, Manyal, 11553, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • intact arches, no missing teeth, and no TMD disorder.

Exclusion criteria

  • patients with less than 24 natural teeth, the presence of active orthodontic treatment, as it could interfere with the data acquisition process, the presence of fixed restorations, severe malocclusion, and those with orofacial pain.

Treatment and study plan

osscluSense with customized centering tray

Device

A customizable centering tray is a thermoplastic or 3D-printed tray designed to hold the OccluSense sensor straight and centered between arches

Primary outcomes

  1. total number of occlusal contacts recorded by the device

    Time frame: this study has unique characteristics. Each participant underwent two set of occlusal recordings with one week interval between the intervention and control toto minimize the risk of muscle fatigue. the outcomes were measured and analyzed instantly

  2. total contact area and the Number of contact points

    Time frame: two visits with one week interval

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Clinical Evaluation of the Validity of Occlusal Contact Area Measurement Using OccluSense With Versus Without Customizable Stabilizing Tray

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jan 26, 2026
Registry last updated
Jan 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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