OSA

9

Review clinical trials related to OSA. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Effect of Interval Exercise on Functional Outcomes in Veterans With COPD and OSA

The term "Overlap Syndrome" (OS) is used to describe the presence of both chronic obstructive pulmonary disease (COPD) and obstructive sleep apnea (OSA) in a single patient. Due to premature aging, patients with OS are prone to developing functional decline up to 20 years earlier than the general population. The International Classification of Functioning, Disability and Health (ICF) evaluates functional status in chronic pulmonary disease globally in 5 domains. The investigators propose to study validated outcomes in 3 of these domains: 1) participation in life situations; 2) physical activity; and 3) cardiovascular health. The investigators long-term goal is to develop an exercise strategy tailored to Veterans with OS which will reduce the risk of functional decline through increased PA.

Participants needed: 28
Trial details
Biological sex: AllType: InterventionalSponsor: VA Office of Research and DevelopmentUpdated: Apr 24, 2026Locations: 1
Eligibility criteria

Diagnosis of COPD and OSA, i.e., Overlap Syndrome Diagnosis of Overlap Syndrome... [+1]

CAD, as defined by anyone of the following: history of CABG, prior positive stre... [+4]

Status: Recruiting

Impact of Muscle Training Device on Non-Severe OSA

The goal of this clinical trial is to test for the efficacy of the newly invented device #DidgeriTU with non-severe obstructive sleep apnea. The main question it aims to answer is: • Can DidgeriTU reduce apnea events in patients with non-severe obstructive sleep apnea? Researchers will compare DidgeriTU with a sham device to see how the apnea event has changed. Participants will: * Use DidgeriTU or sham device for 3 month * Do an online questionnaire once a month during the study * Home sleep test, lung function test, and tongue strength test at the start and end of the study

Participants needed: 76
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Thammasat University HospitalUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

Patients diagnosed with mild to moderate obstructive sleep apnea. [+2]

Patients with an average apnea-hypopnea index (AHI) of <4 or >29 events per hour... [+6]

Status: Recruiting

The Use of Entropy to Assess Sleep Disordered Breathing in Chronic Respiratory Disease

Research is being conducted into chronic respiratory diseases, including chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease, and bronchiectasis. The investigation specifically focuses on sleep-disordered breathing (SDB) in individuals with chronic respiratory disease. SDB encompasses a range of conditions, the most common of which is obstructive sleep apnoea. In obstructive sleep apnoea, periodic pauses in breathing (apnoea) lead to reduced blood oxygen levels. To detect these events, patients typically undergo sleep studies that involve monitoring oxygen saturation, heart rate, and respiratory patterns during sleep. When chronic respiratory disease and SDB coexist, breathing disturbances during sleep may be exacerbated. To identify SDB, sleep studies are commonly used to assess oxygen levels, heart rate, and breathing patterns. The objective of this research is to identify differences between patients with chronic respiratory diseases who have SDB and those who do not. This will be achieved by analysing sleep study data using a novel analytical approach. The aim is to determine whether this method can yield more detailed insights into the underlying pathophysiology of these conditions.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University College, LondonUpdated: Jul 11, 2025Locations: 1
Eligibility criteria

All adult patients (≥ 18years) with chronic respiratory disease with/without SDB... [+3]

Patients who are under 18 years of age at the time of the index study. [+2]

Status: Recruiting

Diagnosing Obstructive Sleep Apnea Using Electromyography of the Muscles of the Mouth

The investigators will establish how well a novel, quick, and painless way of measuring muscle activity from the mouth and throat works for detecting sleep apnea. This technology is called transmembraneous electromyography (tmEMG). Leveraging two technologies, a new probe capable of recording muscle activity by lightly touching the muscle, as well as a machine learning model for signal interpretation, the investigators will conduct an initial observational feasibility study in phase 1, followed by a larger observational cohort study in phase 2 to assess the performance of deep learning enhanced tmEMG. The study will address a critical unmet need in sleep apnea diagnostics: the availability of an inexpensive, accurate diagnostic test for screening at point of care.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: University of California, San DiegoUpdated: Apr 25, 2025Locations: 1
Eligibility criteria

Age 18 years or older [+3]

Current use of OSA therapy, including PAP (positive airway pressure) or non-inva... [+13]

Status: Recruiting

Detecting Heart Rate, Respiration, and Sleep With the Sleeptracker-AI Under-mattress Monitor

The objective of this study is to simultaneously acquire sleep and breathing data using the under-mattress Sleeptracker (The Sleeptracker-AI Monitor (Fullpower Technologies, California, USA) during routine PSGs in patients who attend the Woolcock Institute for undergoing investigation for possible obstructive sleep apnoea (OSA).

Participants needed: 100
Trial details
Age: 20-90Biological sex: AllType: ObservationalSponsor: Woolcock Institute of Medical ResearchUpdated: Mar 28, 2025Locations: 1
Eligibility criteria

Adults aged 20-90 years old at time of assessment. [+3]

Unable to understand study procedure. [+1]

Status: Recruiting

Reversible Effect of Falling Ventilatory Drive in Drive-dependent OSA

Obstructive sleep apnea (OSA) is a highly prevalent disorder that has major consequences for cardiovascular health, neurocognitive function, risk of traffic accidents, daytime sleepiness, and quality of life. For years, a "classic" model of OSA has been used to describe the disorder, which fails to capture it's complexity. Recently, a model for OSA called drive-dependent OSA was discovered be more prevalent in the OSA population. The drive-dependent subgroup benefits exclusively from increased ventilation, increased dilator muscle activity, and reduced event risk when drive spontaneously rises. This study seeks to provide direct evidence that reducing the loss of drive prevents the loss of ventilation, pharyngeal muscle activity, and thus the onset of OSA respiratory events, specifically in "drive-dependent" but not "classic" OSA. This will be achieved using CO2 delivered at precise times during breaths in sleep to prevent loss of overall ventilatory drive.

Participants needed: 36
Trial details
Age: 21-80Biological sex: AllType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Mar 19, 2025Locations: 1
Eligibility criteria

Diagnosed OSA (AHI≥15 events/h reported in a PSG performed within 1 year) or Sus... [+1]

Any unstable medical conditions [+10]

Status: Recruiting

Lifestyle Changes in PCOS with OSA and NAFLD

Complain of obstructive sleeping apnea and fatty liver is common in PCOS women so lifestyle changes are recommended

Participants needed: 40
Trial details
Age: 30-40Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Sep 19, 2024Locations: 2
Eligibility criteria

forty women [+4]

cardiac insult [+3]

Status: Recruiting

Long-term Benefits of CPAP or MAD Treatment on the Sleep of OSAS Patients

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.

Participants needed: 400
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: ResMedUpdated: May 21, 2024Locations: 9
Eligibility criteria

Patient already included in the SunSAS study (No. ID/RCB: 2021-A01827-34) or Pat... [+5]

Patient previously treated for OSAS by CPAP or MAD during the last five years [+4]

Status: Recruiting

Acetazolamide as a Means to Mitigate Falling Ventilatory Drive and Drive-dependent OSA

Obstructive sleep apnea (OSA) is a highly prevalent disorder that has major consequences for cardiovascular health, neurocognitive function, risk of traffic accidents, daytime sleepiness, and quality of life. For years, a "classic" model of OSA has been used to describe the disorder, which fails to capture it's complexity. Recently, a model for OSA called drive-dependent OSA was discovered be more prevalent in the OSA population. This drive-dependent OSA is due to ventilation instability that occurs during respiratory events however these individuals have spontaneous increases in drive during respiratory events that stabilize their airway (i.e., via improving upper airway muscle activity) and reduce the risk of respiratory events in people with OSA. Therefore, by stabilizing the ventilatory drive, OSA should be treatable. Acetazolamide is a pharmacological ventilatory stimulant and has been previously shown to reduce OSA severity. As such in this study, the goal is to demonstrate acetazolamide improves OSA severity in 'drive-dependent' OSA people by improving drive-related pharyngeal obstructions compared to the 'classic' OSA people.

Participants needed: 36
Trial details
Phase: Phase 1, Phase 2Age: 21-80Biological sex: AllType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Mar 4, 2024Locations: 1
Eligibility criteria

Ages 21-80 years [+2]

Any unstable medical condition [+22]