Obstructive Sleep Apnea Of Adult

18

Review clinical trials related to Obstructive Sleep Apnea Of Adult. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Clinical Trial of the Cryosa System for the Treatment of Obstructive Sleep Apnea

This is a prospective, multicenter, non-randomized single-arm safety and performance study to collect data to evaluate the safety of the Cryosa procedure to treat obstructive sleep apnea (OSA) in patients with moderate to severe OSA. The study will also evaluate the chronic performance of the Cryosa system and collect clinical measures for therapy effectiveness that will be used to demonstrate safety and effectiveness in the next clinical study.

Participants needed: 25
Trial details
Age: 22-70Biological sex: AllType: InterventionalSponsor: Cryosa, Inc.Updated: Apr 30, 2026Locations: 9
Eligibility criteria

Age 22 - 70 years [+5]

Contraindication to general anesthesia or in the opinion of the Investigator wou... [+34]

Status: Recruiting

Cerebral Blood Flow and Ventilatory Responses During Sleep in Normoxia and Intermittent Hypoxia

A prospective double blind, placebo-controlled, randomized cross-over trial to evaluate the effect of lowering cerebral blood flow on the ventilatory chemoreflexes (acute hypoxic and hypercapnic ventilatory responses).

Participants needed: 12
Trial details
Phase: Phase 1, Phase 2Age: 18-45Biological sex: AllType: InterventionalSponsor: University of CalgaryUpdated: May 1, 2026Locations: 1
Eligibility criteria

Healthy adults [+4]

Cerebrovascular, cardio-respiratory, renal and metabolic diseases [+4]

Status: Recruiting

Continuous Positive Airway Pressure (CPAP) for Sleep Apnea in Pregnancy

A randomized controlled trial of 1,500 women to assess whether treatment of obstructive sleep apnea with continuous positive airway pressure (CPAP) in pregnancy will result in a reduction in the rate of hypertensive disorders of pregnancy.

Participants needed: 1,500
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: The George Washington University Biostatistics CenterUpdated: Apr 6, 2026Locations: 14
Eligibility criteria

Singleton gestation. Twin gestation reduced to singleton, either spontaneously o... [+2]

Previously prescribed, current or planned therapy for sleep apnea. [+17]

Status: Recruiting

Melatonin's Effect on Nighttime Blood Pressure and Sleep in OSA Patients (MEBP-OSA)

The goal of this clinical trial is to learn if melatonin works to treat comorbid insomnia in adults with OSA and nocturnal non-dipping blood pressure pattern. The main question it aims to answer is: Does melatonin maintain sleep during night and recover the dipping blood pressure pattern?

Participants needed: 50
Trial details
Phase: Phase 4Age: 18-60Biological sex: AllType: InterventionalSponsor: Instituto Nacional de Ciencias Medicas y Nutricion Salvador ZubiranUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Polisomnographic diagnosis of Obstructive Sleep Apnea

Use of sleep or psychiatric medication [+2]

Status: Recruiting

OSA Risk Level in Dental Patients and Correlation With Complications After General Anesthesia

Obstructive sleep apnea (OSA) is a sleep-related respiratory dysfunction. The prevalence of OSA is increasing with the increasing rates of obesity and elderly population worldwide. Perioperative anesthesia management should be adjusted to improve patient safety in patients with OSA. In OSA patients, positive pressure ventilation support may be required in the preoperative period, various ventilation strategies may be required in the intraoperative period, different pharmacologic agents may need to be avoided, and intensive care unit follow-up or noninvasive ventilation support may be required in the postoperative period. However, it is reported that a significant percentage of OSA patients remain undiagnosed. ASA (American Society of Anesthesiologists) has reported the criteria that should be questioned in order to determine the risk of patients in terms of OSA and to initiate the diagnostic process in risky patients and to make appropriate anesthesiologic arrangements in the perioperative period. In addition, the STOP-BANG assessment scale, which is widely used all over the world in OSA risk assessment, is also used in OSA risk assessment. It is thought that dental caries and extraction needs may be higher in OSA patients, especially since open-mouth sleeping accompanies the situation. In this respect, it is also important for patients to be diagnosed with OSA as it may prevent dental damage due to open-mouth sleeping in the future. Identifying patients at risk for OSA and directing them to the diagnostic process is very important for patient safety. Within the scope of the study, the criteria recommended by ASA and STOP-BANG score will be evaluated and recorded. Risk stratification in terms of STOP-BANG questionnaire and ASA criteria will be done separately for each patient and for each classification method. Patients at high risk will be consulted to the relevant medical department in the preoperative period for further investigation and treatment. In addition, it is aimed to correlate the risk levels determined in the study with postoperative respiratory complications and recovery time.

Participants needed: 240
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Kırıkkale UniversityUpdated: Mar 20, 2026Locations: 2
Eligibility criteria

Patients between 18-80 years of age who apply to the anesthesia clinic for denta... [+1]

Individuals who do not want to participate in the study [+2]

Status: Recruiting

Vascular Endothelial Dysfunction in Sleep Apnea

This double-blind placebo-controlled parallel group randomized study design will be used to test whether 4 weeks of atorvastatin 10 mg daily reduces levels of inflammatory markers in OSA patients treated with CPAP (standard of care). The purpose of this study is to investigate: 1) whether statins reduce endothelial inflammation and pro-thrombotic conditions in OSA, including in patients adherent to CPAP (Aim 1); and 2) whether statins reduce endothelial inflammation and pro-thrombotic conditions by improving endothelial cholesterol metabolism and trafficking in OSA (Aim 2).

Participants needed: 110
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Columbia UniversityUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

Aged ≥18 years [+1]

A history of coronary artery disease, heart failure, stroke, diabetes, malignanc... [+1]

Status: Recruiting

A Cross-sectional Study Examining Adipose Tissue in Obstructive Sleep Apnea

Studies show that sleep apnea increases the risk of cardiovascular disease and is associated with obesity. However, it is unclear how sleep apnea affects fat tissue. Studies have shown that fat tissue is likely involved in developing cardiovascular disease. The purpose of this study is to see how sleep apnea changes fat tissue.

Participants needed: 120
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Mayo ClinicUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

BMI ≤40 kg/m2 [+6]

Vulnerable study population will be excluded [+6]

Status: Recruiting

Impact GLP-1 Agonists Following Bariatric

Glucagon-like peptide 1 (GLP-1) is a hormone that helps regulate blood glucose levels through improved insulin sensitivity and release of insulin from the pancreas, control hunger, induce satiety and plays a role in the metabolic health of a person. GLP-1 receptor agonists (GLP1-RAs) have been shown to be effective in achieving weight loss in patients with type 2 diabetes while improving blood glucose control. Bariatric surgical procedures have been shown to be effective in treating obesity as well as superior to best medical therapy for treatment of diabetes not just through restriction of calories but also through a positive impact in modifications of gut hormones, changes in circulating bile acids, modifications in the gut microflora as well as other undefined mechanisms. The combined benefits of GLP1-RAs with bariatric surgery have only been studied to a limited effect. In this randomized trial, the effects of continuation or discontinuation of GLP1-RA therapy in patients undergoing bariatric surgery will be determined. We will compare changes in weight, metabolic determinants including circulating bile acids and gut microbiome, psychological determinants of eating behavior, and adverse side effects in patients who continue vs discontinue therapy. Given differences in metabolic and clinical outcomes in patients undergoing vertical sleeve gastrectomy (VSG) and Roux-en-Y gastric bypass (RYGB), both surgical groups will be examined. The study will be conducted at a high volume bariatric surgical program where patients will undergo randomization at the time of final clinic visit prior to surgery to continue or discontinue GLP1-RA. It is hypothesized that participants who continue GLP1-RA therapy after bariatric surgery will lose more weight with improved blood glucose control than those who discontinue therapy. Furthermore, changes in gut microbiome and circulating bile acids, known determinants of metabolic health, will be modified to a differential extent in those who are on GLP1-RAs vs those where GLP1-RAs are discontinued. Understanding the role these medications play in not only clinical outcomes after metabolic surgery but potential metabolic mechanisms by which surgery improves patient's metabolic health could help people with obesity and type 2 diabetes make informed decisions about their treatment options as well as advise providers on the continuation of these medications in the perioperative and postoperative period.

Participants needed: 150
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of Missouri-ColumbiaUpdated: Jan 22, 2026Locations: 1
Eligibility criteria

Greater than 18 years of age [+8]

Pregnant patient [+6]

Status: Recruiting

Effect of Inspiratory Muscle Training in Obstructive Sleep Apnea Syndrome.

Sleep apnea-hypopnea syndrome is a sleep-related respiratory disorder characterized by partial or total interruptions in breathing during sleep. The majority of syndromes involve an obstructive mechanism (OSA), caused by a reduction in the caliber of the upper airway (UA), most often associated with hypotonia of the surrounding muscles, preventing air from entering the UA during inspiration. The clinical consequences of this syndrome are excessive fatigue and daytime sleepiness, which have a negative impact on the quality of life of patients. Despite the positive results on apnea-hypopnea index and daytime sleepiness of continuous positive airway pressure (today's reference treatment), its 3-year compliance rate (i.e 59.9% according to a study by Abdelghani et al points to the need to develop other associated therapies. Several studies have demonstrated the efficacy of physiotherapy, such as physical activity and oro-pharyngeal muscle strengthening, notably on the apnea-hypopnea index and daytime sleepiness measured by the Epworth scale. Few studies have investigated the effect of inspiratory muscle training (IMT), even though the use of the inspiratory musculature (i.e. the diaphragm) is a means of supplementing the peri-pharyngeal muscles, as it helps to maintain the permeability of the upper airways. Inspiratory muscle training (IMT) could therefore be considered as part of the physiotherapeutic management of the OSA. The heterogeneity of current results concerning IMT in OSA , but above all the lack of evidence that it is dangerous, means that new clinical studies could be carried out in an attempt to demonstrate its efficacy. Our research hypothesis is therefore as follows: Implementing an inspiratory muscle strengthening protocol in patients suffering from OSA can reduce daytime sleepiness.

Participants needed: 58
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Régional d'OrléansUpdated: Dec 30, 2025Locations: 1
Eligibility criteria

patients over 18 years of age with [+1]

Sleep apnea of neurological or mixed origin, [+6]

Status: Recruiting

Cardiometabolic Risk Effects of Short-term Cessation of Neurostimulation Therapy

Hypoglossal nerve stimulation (HGNS) is an implantable therapy that treats obstructive sleep apnea. The study will evaluate the effect of this treatment on cardiovascular and metabolism-related measures to see if it affects patients' risk of medical problems associated with obstructive sleep apnea (OSA).

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Columbia UniversityUpdated: Jul 10, 2025Locations: 1
Eligibility criteria

English-speaking adults (18+ years) who have met surgical efficacy criteria with... [+2]

Chronic use of opiate medications, illicit drugs, or alcohol dependency [+5]

Status: Recruiting

Comprehensive Respiratory Training Exercise Program in Obstructive Sleep Apnea

Obstructive sleep apnea (OSA) is a multi-factorial sleep disorder. Complete collapse or partial collapse in the airway increases the risk of developing cardiovascular and kidney-related disease in OSA patients. Resulting in an increase in medical expenses and workload for the healthcare worker. Multilevel of upper airway muscles especially the genioglossus muscle showed to contribute to airway obstruction as it fatigues easily. The endurance level of OSA patients was shown to be significantly lower. Therefore, the goal of this experimental study is to assess the feasibility and effectiveness of a comprehensive respiratory training exercise program on cardiorespiratory endurance, airway muscle function, and sleep parameters in patients with obstructive sleep apnea (OSA). Aside from exploring the therapeutic effect, the results of the study will be used to explore the mechanism of the treatment in relation to the changes in the OSA severity.

Participants needed: 150
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: National Cheng-Kung University HospitalUpdated: Jun 18, 2025Locations: 1
Eligibility criteria

Newly diagnosed with OSA (AHI≥ 5 events per hour) [+2]

Central or mixed types of sleep apnea [+7]

Status: Not yet recruiting

An Extension Study to Assess the Long-term Safety of the Genio® System

The objective of this study is to assess the long-term safety of the Genio® system in adult OSA patients with and without complete concentric collapse of the soft palate who have successfully been implanted with the Genio IS in a Nyxoah sponsored Clinical Investigation. (Serious) Adverse Device Effects and Device Deficiencies in subjects previously implanted with a Nyxoah Genio implantable stimulator (IS) and having the IS still in-situ (with therapy activated or deactivated) will be collected. The main question it aims to answer is: what is the long term safety profile of the Genio System? Participants will be asked to refer back to the site per standard of care and report on any (Serious) Adverse Device Effects and Device Deficiencies that may have occurred.

Participants needed: 39
Trial details
Biological sex: AllType: ObservationalSponsor: Nyxoah S.A.Updated: Jun 4, 2025Locations: 7
Eligibility criteria

Subject voluntarily signed an Informed Consent Form [+1]

None

Status: Recruiting

Smartwatch-Based AI Model for OSA Prediction (SWOSA)

This study aims to develop an artificial intelligence (AI) model for more accurately diagnosing obstructive sleep apnea (OSA) by collecting blood oxygen saturation and other health information during sleep using a smartwatch. OSA is common but often underdiagnosed, and the gold-standard diagnostic test, polysomnography, is costly and time-consuming. Smartwatches can provide a variety of health data, such as sleep patterns, blood oxygen saturation, and heart rate, which can help detect key symptoms and signs of OSA. By developing an AI model that uses smartwatch data to screen for OSA, this study seeks to offer a cost-effective and accessible diagnostic method, ultimately contributing to the early detection and improved treatment rates of OSA.

Participants needed: 147
Trial details
Age: 22-85Biological sex: AllType: ObservationalSponsor: Seoul National University HospitalUpdated: May 15, 2025Locations: 1
Eligibility criteria

Men and women aged 22 to 85 years who visited Seoul National University Hospital...

Patients previously diagnosed with sleep apnea who are currently undergoing trea... [+7]

Status: Recruiting

Developing a Treatment Clustering System for Obstructive Sleep Apnea Using Polysomnographic Physiological Signals

Obstructive sleep apnea syndrome (OSA) is marked by repeated upper airway obstructions during sleep, affecting approximately 14% of men and 5% of women aged 30-70 years. However, precise clinical prediction tools for selecting optimal treatment strategies are lacking. This study aims to develop an automated treatment clustering system using artificial intelligence to classify patients based on etiology into (i) anatomical factors, (ii) reduced muscle responsiveness, and (iii) other non-anatomical factors. This system will analyze physiological sleep assessments, such as electromyography (EMG) and pneumotachographs, from a retrospective polysomnography (PSG) database. Cross-validation will be conducted on new OSA patients undergoing various management strategies, including surgical intervention, CPAP therapy, and oropharyngeal training (delivered face-to-face or via telerehabilitation). This system aims to enhance clinicians' ability to predict treatment success rates and improve patient outcomes.

Participants needed: 150
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: National Cheng-Kung University HospitalUpdated: Aug 6, 2024Locations: 1
Eligibility criteria

OSA patients [+1]

BMI≧ 32 [+10]

Status: Not yet recruiting

Obstructive Sleep Apnea Treatment in Serious Mental Illness

Serious mental illnesses (SMI) like schizophrenia and bipolar disorder are two of the most disabling and costly chronic illnesses worldwide. A high proportion of adults with schizophrenia and bipolar disorder have sleep disorders, like obstructive sleep apnea (OSA), but tend to be underdiagnosed and undertreated compared to the general population. This study aims to examine feasibility, acceptance, and impact of OSA treatment and how it affects cognitive function in people with SMI.

Participants needed: 300
Trial details
Age: 40-70Biological sex: AllType: InterventionalSponsor: University of California, San DiegoUpdated: Jul 10, 2024Locations: 1
Eligibility criteria

lifetime absence of major psychiatric illness [+6]

DSM-IV-TR diagnosis of active alcohol or other substance abuse or dependence in... [+5]

Status: Recruiting

Changes in Difficult Airway Markers After Surgery for Obstructive Sleep Apnoea Syndrome

This study investigates the changes in difficult airway markers at 6 months post operatively in patients undergoing obstructive sleep apnoea surgery

Participants needed: 42
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kocaeli City HospitalUpdated: Jun 7, 2024Locations: 1Duration: 1 Year
Eligibility criteria

Age between 18-65 [+2]

Verbal and written consent cannot be obtained

Status: Recruiting

Efficacy of Oropharyngeal Exercises for Patients With Obstructive Sleep Apnea Using Mandibular Advancement Device

Oropharyngeal muscle training has emerged as a novel adjunctive treatment approach, involving training of the swallowing muscle group and tongue muscles to prevent tongue collapse, reduce tongue base volume during sleep, and strengthen muscle tension. Therefore, the objective is to assess changes in oropharyngeal muscle strength, ultrasonographic tongue morphology, severity of sleep related breathing interruptions, clinical symptoms, and correlations among these factors. Oropharyngeal muscle training for patients with residual OSA using MAD can significantly 1. increase muscle strength and endurance. 2. reduce the severity of sleep-related breathing interruptions. 3. decrease clinical symptoms. 4. improve tongue morphology.

Participants needed: 20
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: National Cheng-Kung University HospitalUpdated: Mar 21, 2024Locations: 1
Eligibility criteria

OSA patients [+2]

Body Mass Index (BMI) ≧ 35 [+6]

Status: Recruiting

Management of Obstructive Sleep Apnea Syndrome by Expansion Palatoplasty

The study will be conducted to evaluate the outcome of expansion palatoplasty in management of OSAS.

Participants needed: 30
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: ET ZariefUpdated: Feb 28, 2024Locations: 1
Eligibility criteria

Adult patients. [+3]

• Refusing enrollment into the study. [+10]