Efficacy Study of the Medical Device TRP Snorless™ in the Treatment of Snoring

Inclusion Criteria: * Man or woman ≥ 18 years and ≤ 65 years at the time of signing informed consent * Listed as continuous snorer (snoring at least 4 nights/week) * Answer "Extremely loud" or "very loud" to question 1 of SBPS at screening * Answer "very severe" or "severe" to question 2 of SBPS at screening * Answer "extremely" or "quite a bit" to question 3 of SBPS at screening * Dated and signed informed consent * BMI ≤ 35 Exclusion Criteria: * Severe Mandibular retrognathia and micrognathia * Narrow and deep palate (less than 3 cm wide) * Lack of three consecutive teeth in the area of (15-16-17-18) or (25-26-27-28). * Lingual or labial short frenulum (the tongue cannot reach the upper incisors when mouth can be opened for two fingers) * Intolerable gag reflex * Known nasal septal deviation * Neck circumference \> 46 cm * Patient currently treated for OSA * Patient with AHI≥30 events/hour or with AHI\>15 and (SFI) Sleep Fragmentation Index \> 20 * Patient currently treated for central sleep apnoea * Addiction to alcoholic beverages (5 drinks per day per NIAAA) * Under constant pharmacological treatment for depression, anxiety, chronic pain, insomnia * Hypertrophy of tonsils * Macroglossia * Hypertrophy of uvula * Primary gastroesophageal reflux * Any other pathology preventing subject from complying with the protocol * Subject with recent oropharyngeal surgery or likely during the study * Mental inability, unwillingness or language barrier precluding adequate understanding of or compliance with study procedures * Pregnancy * Patient with severe Chronic Obstructive Pulmonary Disease * Asthmatic patient under inhaled corticoid therapy