Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05866835

Validation of a Digitalised Intraoral Protection

Validation of a Generic Procedure for the Fabrication of a Custom-made Intra-oral Protection Using an Inter-arch Piece

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
University Hospital, Bordeaux · Academic / Other
Sex
All
Age
16 Years – 35 Years
Healthy volunteers
Accepted

Summary

Type III (custom-made) intra-oral protection (IOP) models represent 13% of IOP worn by amateur rugby club players in France. However, this model is recognized as the most effective when made in accordance with essential health and safety requirements. This observation is at the origin of a new approach that the investigators are proposing with the objective of removing the barriers to access to custom-made IOP. This research is based on the combination of new digital technologies, scanning and 3D printing, to develop a new generation of IOP. This project aims to show the interest of this new generation of "modified unimaxillary" IOP on the ventilation of the athletes and his/her comfort when he/she evolves with his IOP in place

Detailed description

Type III (custom) Intra Oral Protection (IOP) models represent 13% of IOP worn by amateur rugby players in France. However, this model is recognized as the most effective when made in accordance with essential health and safety requirements. This under-utilization can be explained by the existence of many barriers to the diffusion of custom-made IOP: 1. Organizational barrier: long fabrication procedure (minimum 3 sessions) requiring qualified people (dental surgeon, dental technician), trained in the technique of making custom IOP and in essential health and safety criteria. 2. Financial barrier: high cost with a selling price of 200€ to 300€ per unit. 3. Technical barriers: * Difficulties in making custom-made IOP for athletes who wear fixed braces (brackets and wire), * Difficulties in improving the impact energy dissipation capacity without affecting the absorption capacity of the custom-made IOP, * Difficulties in individualizing and characterizing the IOP. This observation is at the origin of a new approach proposed in order to remove the barriers to access to custom IOP. Naturally, this project relies on the combination of new digital technologies, scanning and 3D printing, to develop a new generation IOP with : * A simpler and shorter procedure, * A target price accepted by athletes, * "French Association for Standardization"(AFNOR) standards guaranteed, * Compatibility with fixed orthodontic treatments, * Ability to develop new protection strategies, * Ability to improve the athlete's comfort. Currently, the IOP resulting from these technologies are mainly "unimaxillary", i.e. without engagement of the mandibular dental arch and without ventilation space. In order to comply with the Afnor XP S72-427 standard, the project proposes the fabrication of two models of "modified unimaxillary" IOP that ensure the engagement of the mandibular dental arch and the creation of a ventilation space at two different heights, 4mm and 6mm. This project aims to show the interest of this new generation of "modified unimaxillary" IOP on the athlete's ventilation and his comfort when he evolves with his IOP in place. It is based on a population of men and women, minors and adults, practicing a sport at risk of oral trauma and uses a methodology already proven by the research team.

Conditions

Interventions

TypeNameDescription
OTHERManufacture of custom-made IOPManufacture of custom-made "unimaxillary" and "modified unimaxillary" intra-oral protection (IOP) with vertical dimensions of 4 mm and 6 mm. 3D modeling of a IOP based on: * digital recording of the maxillary and mandibular dental arches * mandibular wedging performed with an inter-arch piece * digital recording of the inter-arch position
OTHERVentilation testsRealization of a ventilation test (VO2max) to determine the Maximum Aerobic Speed (MAS). Measurement of ventilatory parameters without IOP and with each IOP : * At rest, standing still. * During a 4 minute run on a treadmill at 50% of MAS. * During a 4-minute run on a treadmill, at a speed corresponding to 70% of MAS
OTHEREvaluation of comfort level:Collection from participants (self-questionnaire)

Timeline

Start date
2023-10-10
Primary completion
2026-01-01
Completion
2026-01-01
First posted
2023-05-19
Last updated
2025-08-08

Locations

3 sites across 1 country: France

Source: ClinicalTrials.gov record NCT05866835. Inclusion in this directory is not an endorsement.