Validation of a Digitalised Intraoral Protection

Официальное название

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

Обзор

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

Подробное описание

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.

Вмешательства

• Другое Manufacture of custom-made IOP
  Manufacture 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
• Другое Ventilation tests
  Realization 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
• Другое Evaluation of comfort level:
  Collection from participants (self-questionnaire)

Первичные конечные точки

• Ventilatory flow per minute [Срок оценки: 3 weeks (W3) after inclusion (W0)]

Вторичные конечные точки (1)

• Confort level [Срок оценки: 3 weeks (W3) after inclusion (W0)]

Критерии участия

Критерии включения

• Subjects between the ages of 16 and 35,
• Subject affiliated to a social security system,
• Subject affiliated with the French Federation of Boxing or Rugby or Football
• Subject having signed a consent form
• For minors, legal guardians having signed the free and informed consent form

Критерии исключения

• Subject with a pathology incompatible with the realization of the trial:

• Absolute contraindications: Recent infarction (wait 5 to 12 days depending on severity), Threat syndrome (lawful test after stabilization - at least 3 days without spontaneous seizures), Resting BP > 200/120 mmHg, Uncompensated heart failure, Third-degree Atrioventricular block, Myocarditis, Pericarditis, Endocarditis, Aortic Dissection, Intracardiac tumor or thrombus, Deep venous thrombosis, Pulmonary Embolism,
• Relative contraindications: Aortic stenosis (formal contraindication if lipothymia, syncope or signs of heart failure), Severe non-revascularized coronary artery disease, Pulmonary arterial hypertension (formal contraindication if primary), Severe rapid ventricular or supraventricular arrhythmias
• Subject under B-mimetic drug treatment,
• Subject with decaying teeth,
• Subject under court protection,
• Subject participating in another research study,
• Subject in pregnancy.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Другое

Центры проведения

Франция · 3 центра

• CHU de Bordeaux — Bordeaux
• CREPS de Bordeaux — Bordeaux
• Institut national du sport, de l'expertise et de la performance (INSEP) — Paris

Идентификаторы

NCT: NCT05866835 · CHUBX 2022/61

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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