Condition: Sleep Apnea Syndrome, Obstructive · Sponsor: University Hospital, Grenoble
The goal of this clinical trial is to determine whether treatment-adjustment decisions based on one night of home monitoring with the Sunrise device are comparable to decisions based on one night of in-laboratory polysomnography (PSG) in adults with obstructive sleep apnea (OSA) who remain insufficiently controlled with continuous positive airway pressure (CPAP) therapy. The main questions it aims to answer are: * Do Sunrise-based assessments lead to similar therapeutic decisions as PSG-based assessments? * Are residual apnea-hypopnea indices measured by Sunrise comparable to those measured by PSG? Participants will complete both assessment sequences in a randomized cross-over design. They will: * Use the Sunrise device for several nights with and without CPAP. * Undergo one night of PSG with and without CPAP. * Have their CPAP therapy reviewed based on the results of each assessment method.
This description comes directly from the study's public registry record.
Marie JOYEUX-FAURE, Pr · +33(0)476767166 · MJoyeuxfaure@chu-grenoble.fr
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| CHU Grenoble Alpes | Grenoble, France | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07530302