This study seeks to compare the clinical efficacy and safety of the novel sedative Remimazolam with Dexmedetomidine in Drug-Induced Sleep Endoscopy (DISE), evaluating their performance in sedation depth stability, incidence of adverse events, and postoperative recovery time, thereby providing evidence-based guidance for sedative selection in OSA patients. Additionally, it aims to develop a model for predicting upper airway obstruction sites by analyzing Polysomnography (PSG) data with artificial intelligence, enhancing diagnostic accuracy and treatment decision-making efficiency for Obstructive Sleep Apnea (OSA) to optimize clinical management.
Age range
18 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Apneic events
Timeframe: from start of sedation to outpatient discharge from postoperative care unit
Bradycardia
Timeframe: from start of sedation to outpatient discharge from postoperative care unit
Hypotension
Timeframe: from start of sedation to outpatient discharge from postoperative care unit
Agitation
Timeframe: from start of sedation to outpatient discharge from postoperative care unit
Surgeon satisfaction score
Timeframe: From start of sedation to outpatient discharge from postoperative care unit
Hypoxic event
Timeframe: From start of sedation to outpatient discharge from postoperative care unit