Obstructive sleep apnea trials may require a recent sleep study (AHI), CPAP intolerance, or a BMI range for medicine studies. Central sleep apnea is a different condition. We do not interpret your sleep study. Sourced from ClinicalTrials.gov. Not a recommendation to join any study.
RecruitingNot a traditional drug phaseBethesda, Maryland
Development of a Wearable Point of Care Monitoring Device for Pediatric Obstructive Sleep ApneaBackground: Obstructive sleep apnea (OSA) occurs when the blockage of the airway causes a person to stop breathing involuntarily for 10 seconds or more throughout the night during sleep. Pediatric OSA can be especially concerning and can have long-term effects.
NCT05052216 · Official ClinicalTrials.gov record · Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
RecruitingNot a traditional drug phaseSan Diego, California
Not a traditional drug phase: Positive Airway Pressure Device for Post Traumatic Stress DisorderSubstance use disorder (SUD) and posttraumatic stress disorder (PTSD) frequently co-occur and having both disorders is associated with greater psychological and functional impairment than having either disorder alone. This is especially true in residential settings where both disorders are more severe than outpatient settings.
NCT05156112 · Official ClinicalTrials.gov record · VA Office of Research and Development
RecruitingNot a traditional drug phaseBeijing
Not a traditional drug phase: Level III portable sleep study for Sleep ApneaThe investigators propose a prospective, watch-and-measure (no experimental treatment required) study to determine the impact of OSA and associated physiological parameters on clinical outcomes in patients with pulmonary hypertension. The prevalence, phenotypes, and predictors of OSA in the setting of pulmonary hypertension will also be investigated.
NCT05595200 · Official ClinicalTrials.gov record · Chinese Pulmonary Vascular Disease Research Group
RecruitingNot a traditional drug phaseTucson, Arizona
Not a traditional drug phase: Positive airway pressure for Obstructive Sleep ApneaThe Effects of Successful OSA TreatmENT on Memory and AD BIomarkers in Older AduLts (ESSENTIAL) study is a 5-year, multicenter randomly assigned open-label trial that will screen 400 cognitively normal older adults recruited from well-established sleep clinics at 4 academic medical centers, with newly diagnosed moderate-severe OSA. An expected 200 OSA patients will be then randomly assigned to one of two groups: i) a 3-month OSA treatment by any combination of PAP, OAT, and positional therapy that results in an "effective" AHI4%\< 10/hour and AHI3A\<20/hour (see below); ii) a waitlist control group to receive treatment at the conclusion of the 3-month intervention period.
NCT05988385 · Official ClinicalTrials.gov record · California Pacific Medical Center Research Institute
RecruitingNot a traditional drug phaseMiami, Florida
Not a traditional drug phase: Standard of Care for Sleep ApneaThe purpose of this research is to see how effective the Personalized obstructive sleep apnea (OSA) Treatment Adherence Model called PRAISE is in helping the patient stick to the physician recommended OSA treatment plan Positive Airway Pressure (PAP).
NCT06089161 · Official ClinicalTrials.gov record · University of Miami
RecruitingPhase 4Columbia, Missouri
Phase 4: testing GLP-1 receptor agonist for Morbid ObesityGlucagon-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.
NCT06132477 · Official ClinicalTrials.gov record · University of Missouri-Columbia
RecruitingNot a traditional drug phaseMorrisville, North Carolina
Not a traditional drug phase: testing Sunosi (solriamfetol) for NarcolepsyThe SUNOSI (solriamfetol) Pregnancy Registry is a US- and Canada-based prospective, watch-and-measure (no experimental treatment required) study to measure the safety of solriamfetol exposure during pregnancy in women with a diagnosis of narcolepsy or obstructive sleep apnea (OSA).
NCT06413420 · Official ClinicalTrials.gov record · Axsome Therapeutics, Inc.
RecruitingNot a traditional drug phaseHong Kong
Microbiome and Metabolomics Profiling in Children With OSAObjectives: Obstructive sleep apnoea (OSA) exhibits variable susceptibility to end-organ morbidities. Previous studies suggest that physiological sequelae in individuals with OSA promote changes in microbiome, which also interact with metabolic and inflammatory mediators.
NCT06452992 · Official ClinicalTrials.gov record · Chinese University of Hong Kong
RecruitingPhase 1 / Phase 2Chicago, Illinois
Phase 1 / Phase 2: testing Dronabinol for Obstructive Sleep ApneaThis is an open-label trial that tests the effectiveness of Dronabinol in treating obstructive sleep apnea (OSA). All participants will take oral Dronabinol for two weeks.
NCT06477952 · Official ClinicalTrials.gov record · VA Office of Research and Development
RecruitingNot a traditional drug phaseToulouse
Not a traditional drug phase: Mandibular Advancement Device for Obstructive Sleep Apnea SyndromeThis research addresses obstructive sleep apnea syndrome (OSAS), affecting 6-12% of French adults, often treated with mandibular advancement devices (MADs). MADs may lead to occlusal modifications, causing a 50% treatment abandonment rate.
NCT06576310 · Official ClinicalTrials.gov record · University Hospital, Toulouse
RecruitingNot a traditional drug phaseBrussels
Not a traditional drug phase: Physiotherapist assessment for Obstructive Sleep Disordered BreathingThis study investigates the hypothesis that, in children, tongue motor functions can predict both the anatomical site and the degree of upper airway obstruction contributing to obstructive sleep-disordered breathing.
NCT06792045 · Official ClinicalTrials.gov record · Université Catholique de Louvain
RecruitingNot a traditional drug phaseIstanbul
Not a traditional drug phase: Structured Pre-Sleep Exercise for Apnea, ObstructiveObstructive Sleep Apnea Syndrome (OSAS) is commonly treated with CPAP devices, but adherence rates are low. Exercise has been shown to strengthen respiratory muscles, improve upper airway function, and enhance sleep quality.
NCT07214636 · Official ClinicalTrials.gov record · Medipol University
RecruitingNot a traditional drug phaseShatin
Not a traditional drug phase: Myofunctional therapy for Obstructive Sleep Apnea (OSA)Myofunctional therapy (MFT) has been proposed as an added on top of your current treatment therapy for obstructive sleep apnoea (OSA) in children. Some studies have reported improved sleep parameters and reduced oral breathing after MFT.
NCT07249944 · Official ClinicalTrials.gov record · Chinese University of Hong Kong
RecruitingPhase 3Cullman, Alabama
Phase 3: testing Eloralintide for Sleep Apnea, ObstructiveThe purpose of the studies is to measure the how well it works and safety of eloralintide in participants with moderate-to-severe obstructive sleep apnea and obesity or overweight. YDAO is a master protocol designed to support two independent studies: YSA1 and YSA2.
NCT07369011 · Official ClinicalTrials.gov record · Eli Lilly and Company
RecruitingNot a traditional drug phaseTainan, Taiwan
Not a traditional drug phase: Brief Behavioral Therapy for Insomnia (BBTi) for Comorbid Insomnia and Sleep ApneaThis study investigates the how well it works of a wearable voice-guided Brief Behavioral Therapy for Insomnia (BBTi) combined with a smart eye-mask device for individuals with Comorbid Insomnia and Sleep Apnea (COMISA). The four-year study comprises three phases: (1) exploration of cognitive-emotion regulation-arousal system mechanisms in COMISA and pilot BBTi intervention testing, (2) development and usability testing of an integrated smart eye-mask with BBTi voice-guided modules, and (3) a multi-center randomly assigned controlled trial (RCT) evaluating the combined BBTi plus smart eye-mask intervention versus BBTi alone, smart eye-mask alone, and standard sleep hygiene education in 160 COMISA participants.
NCT07521319 · Official ClinicalTrials.gov record · National Sun Yat-sen University
RecruitingPhase 2Chula Vista, California
Phase 2: testing IHL-42X: 2.5 mg dronabinol + 125 mg acetazolamide for Obstructive Sleep Apnea (OSA)The goal of this randomly assigned, neither you nor the study doctors know who gets the real treatment, multi-dose crossover clinical trial is to determine the safety and how well it works of IHL-42X in subjects with obstructive sleep apnea. The primary endpoint is: Change in AHI4 at the end of each treatment period compared to baseline (each treatment period is 28 days).
NCT07635563 · Official ClinicalTrials.gov record · Incannex Healthcare Ltd
RecruitingPhase 4Tucson, Arizona
Phase 4: testing Atomoxetine-oxybutynin for Obstructive Sleep Apnea (OSA)Researchers want to identify which treatments for obstructive sleep apnea (OSA) work best and are easiest for patients to use consistently. Eligible you would be randomly assigned one of three OSA treatments: traditional PAP therapy, a dental device, or a combination of two FDA-approved medications (atomoxetine and oxybutynin) that are currently approved for other conditions.
NCT07679282 · Official ClinicalTrials.gov record · Sairam Parthasarathy
RecruitingNot a traditional drug phaseHenderson, Nevada
Not a traditional drug phase: The study will assess the feasibility of incorporating the PLATO questionnaire into a dental sleep practice. The PLATO questionnaire was developed as a patient reported outcome measure for Obstructive Sleep Apnea (OSA)Prospective, real-world watch-and-measure (no experimental treatment required) study in a dental sleep practice to assess the feasibility of incorporating the PLATO into a dental sleep practice and applicability for patients who are undergoing oral appliance therapy for the treatment of obstructive sleep apnea(OSA). The PLATO questionnaire was recently developed by the American Academy of Sleep Medicine specifically for use in patients with obstructive sleep apnea.
NCT07789834 · Official ClinicalTrials.gov record · Nevada Dental Sleep
RecruitingNot a traditional drug phaseNew Taipei City
Not a traditional drug phase: fingertip pulse oximeter for Pediatric Obstructive Sleep ApneaThis study aims to develop a multimodal data-driven model integrating multiple noninvasive physiological signals to assess the severity of pediatric sleep-disordered breathing, using standard clinical sleep study results as the reference.
NCT07805486 · Official ClinicalTrials.gov record · Fu Jen Catholic University
RecruitingPhase 3Cullman, Alabama
Phase 3: testing Berobenatide for ApneaThis study is being done to learn about the safety and effects of a study medicine called berobenatide (bear-oh-BEN-uh-tide). The study will see if berobenatide can help adults with breathing problems during sleep (obstructive sleep apnea \[OSA\]) and overweight or obesity who use a breathing machine (positive airway pressure \[PAP\] machine).
NCT07823608 · Official ClinicalTrials.gov record · Pfizer
RecruitingNot a traditional drug phaseSt Louis, Missouri
Not a traditional drug phase: F&P Licorice Mask for Chronic Respiratory ConditionsThis clinical investigation is designed to validate and confirm the overall performance, safety, usability, reliability, and acceptability of the F\&P PAP mask in a home environment.
NCT07826429 · Official ClinicalTrials.gov record · Fisher and Paykel Healthcare
RecruitingNot a traditional drug phaseLiège
Not a traditional drug phase: Cross-sectional assessment for Obstructive Sleep Disordered BreathingThe tongue plays a key role in maintaining upper airway patency during sleep, mainly through the genioglossus, the principal pharyngeal dilator muscle. Its dysfunction may be linked to the development of obstructive sleep-disordered breathing (oSDB), a condition affecting more than one in ten children and associated with cardiovascular and cognitive consequences.
NCT07861230 · Official ClinicalTrials.gov record · Université Catholique de Louvain
RecruitingNot a traditional drug phaseChicago, Illinois
Not a traditional drug phase: Continuous Positive Airway Pressure (CPAP) for PCOSThe goal of this study is to obtain pilot data investigating the effects of sleep apnea on mitochondrial function and cellular metabolism in Polyendocrine Metabolic Ovarian Syndrome (PMOS) patients.
NCT07871149 · Official ClinicalTrials.gov record · University of Chicago
RecruitingNot a traditional drug phaseKaohsiung City
Not a traditional drug phase: Upper airway surgery for OSA for OSA - Obstructive Sleep ApneaDysphagia is a commonly reported complaint among patients with obstructive sleep apnea (OSA), particularly those who have undergone upper-airway (oropharyngeal) surgery. However, how surgical treatment for OSA affects swallowing function and oral function (oral frailty) remains unclear.
NCT07880067 · Official ClinicalTrials.gov record · National Sun Yat-sen University
RecruitingPhase 3Cullman, Alabama
Phase 3: testing Berobenatide for ApneaThis study is being done to learn about the safety and effects of a study medicine called berobenatide (bear-oh-BEN-uh-tide). The study will see if berobenatide can help adults with breathing problems during sleep (obstructive sleep apnea \[OSA\]) and overweight or obesity who are not using a breathing machine (positive airway pressure \[PAP\] machine).
NCT07881757 · Official ClinicalTrials.gov record · Pfizer
RecruitingNot a traditional drug phaseIstanbul, Göztepe
Not a traditional drug phase: Physical Activity Education for Obstructive Sleep ApneaAlthough exercise and physical activity have shown beneficial effects in individuals with obstructive sleep apnea (OSA), evidence regarding the effects of daily physical activity habits on sleep quality and respiratory parameters remains limited. This study aims to investigate these associations in individuals with OSA.
NCT07889154 · Official ClinicalTrials.gov record · Medipol University
RecruitingNot a traditional drug phaseAl Mansurah, Dakahlia Governorate
Not a traditional drug phase: Transcutaneous Electrical Stimulation for Obstructive Sleep Apnea* The aim of this study is to assess the impact of transcutaneous electrical stimulation on polysomnographic findings in obstructive sleep apnea patients. * The hypothesis of the present study is that nocturnal delivery of transcutaneous electrical stimulation of the pharyngeal dilators, in particular the genioglossus, may help in treating the functional loss of the neuromuscular tone with sleep onset to keep the Upper airway patent during sleep which would reduce the severity of OSA as measured by the apnea-hypopnea-index (AHI), so representing an alternative and better-tolerated approach compared to usual care with CPAP.
NCT07891702 · Official ClinicalTrials.gov record · Mansoura University
RecruitingNot a traditional drug phaseBeijing, Beijing Municipality
Development and Clinical Validation of Artificial Intelligence Algorithms for Sleep Staging and Obstructive…In recent years, wearable and contactless devices, including smart rings, smart bands/watches, and smart mattresses, have developed rapidly and can continuously collect multidimensional data such as heart rate, oxygen saturation, respiration, body movement, snoring, body temperature, and environmental parameters. Nevertheless, most current consumer-grade or wellness-oriented devices have not been trained and validated using large polysomnography (PSG)-synchronized reference datasets.
NCT07908160 · Official ClinicalTrials.gov record · Peking University First Hospital
RecruitingNot a traditional drug phaseKarabük
Functional Capacity in Obstructive Sleep ApneaObstructive sleep apnea syndrome (OSAS) is a condition characterized by a deterioration in respiratory function and an increase in the activity of accessory respiratory muscles. This condition can affect patients' use of their upper extremities during daily living activities.
NCT07913139 · Official ClinicalTrials.gov record · Karabuk University
RecruitingNot a traditional drug phaseKaohsiung City
Not a traditional drug phase: Submental transcutaneous neuromuscular electrical stimulation (RS-18) for Obstructive Sleep ApneaThis single-arm pilot study evaluates the feasibility of nightly wearable monitoring with a ring-type sleep monitor during a 4-week home-based program of submental transcutaneous neuromuscular electrical stimulation in adults with obstructive sleep apnea, and describes changes in the ring-derived apnea-hypopnea index, sleep continuity, STOP-Bang score and upper-airway anatomy on CT before and after training.
NCT07921329 · Official ClinicalTrials.gov record · E-DA Hospital
RecruitingNot a traditional drug phaseNew Taipei City, New Taipei City
Development and Validation of a Multimodal Deep Learning Model Using Peripheral Oxygen Saturation and Balli…Obstructive sleep apnea (OSA) is a common sleep disorder associated with cardiovascular, metabolic, and neurocognitive complications. The standard diagnostic test for OSA is in-laboratory polysomnography (PSG), which can be costly, labor-intensive, and inconvenient for repeated or large-scale screening.
NCT07923825 · Official ClinicalTrials.gov record · Fu Jen Catholic University