The REMAP study aims to follow a cohort of 400 patients in around ten sleep centers in France and to collect clinical routine data. The objectives of this study are to investigate the effects of one-year management of OSA by CPAP or MAD on sleep architecture defined by objective macro and micro sleep architecture parameters using a sleep test device. sleep connected at home, to assess the quality of sleep and the quality of life reported by patients. The study will also allow us to define predictive factors for improving sleep quality during OSA treatment.
Study Type
OBSERVATIONAL
Enrollment
400
Fixed-pressure CPAP device for the treatment of sleep apnea with optional humidification and heated circuit. This device is a Class II device. It has a remote monitoring function allowing service providers to track the use of the device.
mandibular device orthosis made to measure from the dental impressions of patients, made by the specialist in the masticatory apparatus for the treatment of sleep apnea.
CHU Angers
Angers, France
RECRUITINGCentre Hospitalier Universitaire Grenoble Alpes
Grenoble, France
RECRUITINGCHU Lyon - Hôpital de la Croix-Rousse
Lyon, France
To determine the evolution of deep slow-wave sleep at one year in OSA patients according to the treatment initiated by continuous positive pressure or mandibular advancement device (MAD).
Objective evolution of deep slow-wave sleep time. Changes collected with a home-connected sleep testing device by comparing data from the initial visit (diagnosis) with data collected at 12 months (± 2 weeks) in a patient treated with CPAP or MAD.
Time frame: 12 months
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Hopital Europeen Marseille
Marseille, France
RECRUITINGAPHP - Pitié-Salpêtrière University Hospital
Paris, France
RECRUITINGAP-HP Bichat
Paris, France
NOT_YET_RECRUITINGCHU Reims
Reims, France
RECRUITINGPolyclinique St Laurent
Rennes, France
RECRUITINGCentre du Sommeil
Saint-Martin-d'Hères, France
RECRUITING