Sleep Disordered Breathing (SDB)

16

Review clinical trials related to Sleep Disordered Breathing (SDB). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

PAH-SDB: Sleep-Disordered Breathing and Outcomes in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a progressive pulmonary vascular disease characterized by increased pulmonary vascular resistance, right ventricular dysfunction, and clinically important morbidity and mortality. Sleep-disordered breathing (SDB) and sleep-related hypoxemia are common in patients with PAH, but their prevalence, physiological determinants, longitudinal trajectories, prognostic significance, and potential role in individualized management remain incompletely defined. PAH-SDB is a prospective, multicenter, observational patient registry enrolling adults with right-heart-catheterization-confirmed World Health Organization Group 1 PAH at pulmonary vascular centers across China. Participants will undergo standardized nocturnal sleep and cardiorespiratory monitoring together with comprehensive PAH assessment, including clinical characteristics, functional status, biomarkers, echocardiography, hemodynamics, treatment, and outcomes. Selected participants may undergo additional polysomnography, cardiac magnetic resonance imaging, wearable monitoring, repeated sleep assessments, or biospecimen collection when available and ethically approved. The registry will characterize the prevalence and phenotypes of sleep-disordered breathing and nocturnal physiological abnormalities; examine their relationships with PAH severity and right ventricular-pulmonary vascular function; determine their value for predicting clinical worsening, hospitalization, transplantation, and mortality; evaluate longitudinal changes in sleep physiology in relation to PAH treatment and disease trajectory; and develop and validate multimodal statistical and artificial-intelligence models for phenotyping, risk prediction, and treatment-response stratification. Clinical management will remain at the discretion of treating physicians, and the registry will not assign PAH or sleep-related therapies.

Participants needed: 1,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chinese Pulmonary Vascular Disease Research GroupUpdated: Oct 1, 2026Locations: 1Duration: 5 Years
Eligibility criteria

Age ≥18 years at enrollment. [+5]

Pulmonary hypertension predominantly attributable to left heart disease (Group 2... [+6]

Status: Recruiting

Start CPAP Therapy in Obstructive Sleep Apnea Patients After Atrial Fibrillation Ablation

Atrial fibrillation (AF) is one of the most common clinical arrhythmias. Catheter ablation is an effective therapeutic strategy; however, recurrence rates remain substantial, ranging from 20% to 45%. Previous studies have established a strong association between obstructive sleep apnea (OSA) and the risk of AF recurrence following ablation. While continuous positive airway pressure (CPAP) is the standard intervention for OSA, and some observational studies suggest it may reduce post-ablation recurrence in patients with comorbid OSA, small randomized controlled trials have failed to confirm a clear benefit, potentially due to poor adherence. This study aims to evaluate the clinical benefit of post-ablation CPAP therapy in AF patients with comorbid OSA. Participants will: * Be randomly assigned to either the CPAP group or the usual care group. * If in the CPAP group, use a CPAP device for 12 months. * Wear an ambulatory ECG recorder for a 7-day period at 3, 6, 9, and 12 months after randomization. * Complete follow-up checkups either at the clinic or over the phone at 1, 3, 6, and 12 months after randomization.

Participants needed: 658
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Beijing Anzhen HospitalUpdated: Oct 5, 2026Locations: 30
Eligibility criteria

Age 18-75 years. [+5]

Secondary AF. [+15]

Status: Recruiting

Early Dental Risk Screening for Pediatric Sleep-Disordered Breathing

This is a prospective, cross-sectional observational study designed to evaluate the Pediatric Sleep Questionnaire (PSQ) as a screening tool for sleep-disordered breathing (SDB) risk in a pediatric dental setting. Children aged 8-13 years will be classified as low- or high-risk for SDB based on PSQ scores and compared using physiologic sleep parameters obtained from a wearable, FDA-cleared home sleep monitoring device, alongside psychosocial assessments and craniofacial measurements derived from lateral cephalometric radiographs. Findings will inform the feasibility and accuracy of incorporating validated SDB screening into routine pediatric dental care.

Participants needed: 60
Trial details
Age: 8-13Biological sex: AllType: ObservationalSponsor: University of North Carolina, Chapel HillUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Ages 8-13 years old [+4]

Diagnosis of a craniofacial syndrome or condition known to significantly alter c... [+4]

Status: Not yet recruiting

Sleep-Assessment in Patients Between High Altitude HA vs. Sea Level LA in Patients With Pulmonary Arterial Hypertension PAH

To study the effect of relocation from high altitude (Quito Ecuador: 2850m) to sea level on sleeping parameters by polygraphy in patients with pulmonary arterial hypertension PAH, who live permanently \>2600m.

Participants needed: 20
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Silvia Ulrich SomainiUpdated: Sep 3, 2026Locations: 1
Eligibility criteria

Adult patients aged 18-80 years and of all genders [+5]

Age <18 years or >80 years [+8]

Status: Not yet recruiting

Sleep-Assessment in Patients Between High Altitude HA vs. Sea Level LA in Healthy Individuals H

To study the effect of relocation from high altitude (Quito Ecuador: 2850m) to sea level on sleeping parameters by polygraphy in healthy individuals, who live permanently \>2600m.

Participants needed: 14
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Silvia Ulrich SomainiUpdated: Sep 3, 2026Locations: 1
Eligibility criteria

Adults aged 18-80 years and of all genders [+3]

Age <18 years or >80 years [+4]

Status: Recruiting

Effect of Adenotonsillectomy on Spinal Curve Magnitude in Children With Sleep-Disordered Breathing

This study aims to determine the effect of adenotonsillectomy (AT) surgery on the progression of spinal curvature in children with mild sleep-disordered breathing (SDB) and concurrent scoliosis, as well as its potential role in preventing the de novo development of scoliosis in children with SDB.

Participants needed: 160
Trial details
Age: 6-15Biological sex: AllType: InterventionalSponsor: Second Affiliated Hospital of Wenzhou Medical UniversityUpdated: May 15, 2026Locations: 1
Eligibility criteria

Age between 6 and 15 years. [+5]

Unwillingness or inability to comply with study procedures. [+14]

Status: Recruiting

Impact of Transcatheter Aortic Valve Implantation and Mitral Valve Repair on Sleep-Disordered Breathing

This prospective observational study aims to investigate the impact of transcatheter aortic valve implantation (TAVI) and transcatheter mitral valve edge-to-edge repair (M-TEER) on sleep-disordered breathing (SDB) in patients with significant valvular heart disease. Patients undergoing TAVI or M-TEER will be evaluated with full polysomnography prior to the intervention and at 6 months follow-up. Changes in sleep parameters, including apnea-hypopnea index (AHI), central and obstructive apnea indices, oxygen desaturation, and sleep architecture, will be assessed. In addition, the study will explore the association between changes in SDB and echocardiographic as well as arrhythmic parameters. The findings are expected to improve the understanding of the interaction between valvular heart disease and SDB and to identify potential benefits of transcatheter interventions on sleep-related outcomes.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Aristides PlaitisUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Adult patients undergoing TAVI or M-TEER [+2]

Inability to undergo sleep study (polysomnography) [+3]

Status: Recruiting

Sleep-disordered Breathing and Neurocognitive Assessment in Children and Young Adults

One of main problems in the management of sleep-disordered breathing (SDB) in children and young adults is their screening, and the absence or the weak correlation between clinical symptoms and polysomnography (PSG). It may be useful to use additional measures together with PSG to improve the detection and characterization of respiratory events during sleep and/or correlation with clinical signs of SDB. The primary objective of the study is to determine whether psychological and neuropsychological test scores correlate with diagnostic PSG results.

Participants needed: 1,200
Trial details
Age: 1-20Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Apr 3, 2026Locations: 1
Eligibility criteria

Patients aged 1 to 20 years with a suspicion of SDB or a high-risk of SDB due to... [+1]

No social insurance [+5]

Status: Not yet recruiting

Metabolic Characteristics and Prognostic Model of Acute Coronary Syndrome Complicated With Obstructive Sleep Apnea

Obstructive sleep apnea (OSA) significantly increases the risk of cardiovascular events in patients with acute coronary syndrome (ACS), yet the underlying metabolic mechanisms remain unclear. This study aims to analyze the metabolic characteristics of ACS patients with OSA using metabolomics based on a prospective cohort. The study intends to construct an artificial intelligence-based risk stratification model to improve prognosis prediction and facilitate precision medicine for this population.

Participants needed: 1,200
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Beijing HospitalUpdated: Feb 9, 2026Duration: 12 Months
Eligibility criteria

Age 18-85 years. [+2]

Cardiogenic shock or cardiac arrest. [+4]

Status: Not yet recruiting

Comprehensive Care of Sleep Disordered Breathing

The Comprehensive Care of Sleep Disordered Breathing study (Care-SDB) is a prospective, multi-center, registry-based cohort study designed to investigate the integrated management of sleep-disordered breathing (SDB). The investigators aim to establish a nationwide SDB cohort and biobank to identify prognostic biomarkers, explore pathogenic mechanisms, and evaluate optimal treatment models. A total of 11,100 adult patients with recent sleep monitoring will be enrolled and followed longitudinally for up to 5 years. Data collection, including clinical outcomes and major adverse events, will be managed via a unified Electronic Data Capture platform. The results from Care-SDB are expected to provide critical evidence-based guidance for the risk stratification, standardized intervention, and personalized management of patients with sleep-disordered breathing.

Participants needed: 11,100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Beijing Anzhen HospitalUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+2]

Estimated life expectancy of less than 3 months. [+2]

Status: Recruiting

Neurostimulation for Sleep Disordered Breathing (SDB)

This is a study to determine if the Lunair Alpha System is safe and effective for treating moderate to severe sleep disordered breathing.

Participants needed: 45
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Lunair MedicalUpdated: Nov 21, 2025Locations: 1
Eligibility criteria

Subject does not tolerate, not compliant to, or have access to alternative Sleep... [+1]

Subject is taking opioids, narcotics, sleep or psychotic medications or suppleme... [+16]

Status: Not yet recruiting

Sleep-Disordered Breathing in Children With Cerebral Palsy at Increased Risk of Respiratory Disorders

Currently, there are few and qualitatively unsatisfactory epidemiological data on the prevalence of sleep-disordered breathing (SDB) in children with cerebral palsy (CP). The investigators aim to conduct a multicentre retrospective study to assess the presence of SDB in children with CP undergoing sleep studies (polysomnography or polygraphy).

Participants needed: 150
Trial details
Age: 0-17Biological sex: AllType: ObservationalSponsor: GUIDO CAMANNIUpdated: Jul 28, 2025Locations: 9
Eligibility criteria

Aged less than 18 at the time of the sleep study [+3]

None

Status: Recruiting

Sleep Disordered Breathing and Multimorbidity: The Xiangya SDB Cohort Study

Sleep disordered breathing (SDB) is one of the most common sleep disorders, including obstructive sleep apnea (OSA), central sleep apnea (CSA), sleep-related hypoventilation, hypoxemia, etc., with OSA being the most prevalent. Also, SDB shows high comorbidities with multisystem diseases. Furthermore, compared to patients with pure SDB, those comorbid with SDB and other disorders like cardiometabolic dysfunction and cognitive impairment experience poorer quality of life, higher rate of disease progression and mortality, and a greater economic burden. Currently, there are limited cohorts to study the associations between SDB and multisystem diseases. The aim of this study is to establish an ambispective clinical cohort for SDB in Xiangya hospital from central-south China (Xiangya Sleep Disordered Breathing Cohort, Xiangya SDB cohort) including retrospective part and prospective part, which covers multi-dimensional data of sleep monitoring, demographic, daily behaviors, clinical manifestations and comorbidities status, life quality, treatment information and evaluation, etc. by self-reported questionnaires and objective assessments and tests. Besides, whole peripheral blood is drawn for following biomarkers study and omics analysis. The main goal is to achieve precise management of SDB and related multimorbidity, containing to early identify risk individuals for multisystem impairment, significantly improve their prognosis and ultimately enhance overall health. In detail: first, to reveal how multisystem impairment related to SDB evolves; second, to identify which indicators closely involve system dysfunction due to SDB; third, to build an efficient model and a cost-effective platform to screen high-risk population and tract therapeutic effect.

Participants needed: 15,000
Trial details
Biological sex: AllType: ObservationalSponsor: Xiangya Hospital of Central South UniversityUpdated: Apr 3, 2025Locations: 1
Eligibility criteria

1) Participants who were suspected of sleep disordered breathing must complete a... [+2]

Participants who refused to participate in this study or whose clinical data was...

Status: Recruiting

Neurostimulation for Sleep Disordered Breathing

This is a first in human study to determine if the Lunair Alpha System is safe and effective for treating moderate to severe sleep disordered breathing.

Participants needed: 45
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Lunair MedicalUpdated: Mar 20, 2025Locations: 1
Eligibility criteria

Subject does not tolerate, not compliant to or have access to alternative Sleep... [+1]

Subject is taking opioids, narcotics, sleep or psychotic medications or suppleme... [+16]

Status: Not yet recruiting

Comparing CPAP and BiPAP for Sleep-Disordered Breathing in People with Cervical Spinal Cord Injuries

Sleep-disordered breathing (SDB) is common in individuals with cervical spinal cord injuries, with studies suggesting prevalence rates ranging from 27% to 62%. The condition often leads to daytime sleepiness, fatigue, and poor participation in rehabilitation. Positive airway pressure therapy can be used to treat the condition; however, some individuals find continuous positive airway pressure (CPAP), which applies the same pressure during inhalation and exhalation, difficult to use. Bilevel positive airway pressure (BiPAP) offers different pressures for inhalation and exhalation, which may be more comfortable and potentially improve adherence in this patient population. However, limited evidence compares CPAP and BiPAP in individuals with cervical spinal cord injuries. This pilot study will enroll 32 adult participants with cervical spinal cord injuries who have moderate to severe SDB (defined as an AHI of 15 events/hour or greater). Participants will be randomly assigned to either CPAP or BiPAP therapy for 4 weeks. Device usage per night will be measured, and data on daytime sleepiness, fatigue, and sleep quality will be collected at baseline, 2 weeks, and 4 weeks. The investigators aim to determine whether BiPAP improves adherence and symptoms compared to CPAP in this patient population.

Participants needed: 32
Trial details
Age: 19+Biological sex: AllType: InterventionalSponsor: University of British ColumbiaUpdated: Feb 10, 2025Locations: 1
Eligibility criteria

Age >= 19 years [+2]

On CPAP or BiPAP prior to spinal cord injury [+1]

Status: Not yet recruiting

Sleep-Disordered Breathing in the Acute Phase After Stroke and Neuropsychiatric Outcomes

In people who have had a stroke or a transient ischemic attack (TIA), it is common to have problems with breathing patterns during sleep, particularly a condition called obstructive sleep apnea. Another common long-term problem after a stroke is post-stroke fatigue, which affects function and quality of life after stroke. There is currently no clearly effective treatment for post-stroke fatigue. We are investigating whether there might be a connection between sleep-related breathing disturbances, and the risk of developing long-term post-stroke fatigue The project is being conducted at Blekingesjukhuset Karlskrona, and inpatients with stroke are asked to participate. Participants are equipped with a sleep analysis pad under the mattress that measures breathing patterns during the night, as well as a wrist-worn device that measures oxygen saturation in the blood. Participants are also asked about their functional level in daily life and any symptoms of obstructive sleep apnea. One year after the stroke, participants are invited for a follow-up visit where we ask about post-stroke fatigue, depressive symptoms, and treatment and investigations related to the stroke. We will then investigate the relationship between sleep-related breathing disturbances, measured early after stroke, and the risk of significant fatigue after the stroke. This could lead to future studies with treatment trials for obstructive sleep apnea in certain individuals with post-stroke fatigue. The study could also lead to potentially increased awareness that these conditions might be connected, which could result in a higher likelihood of detecting treatable obstructive sleep apnea in certain subgroups after stroke.

Participants needed: 340
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Blekinge County Council HospitalUpdated: Feb 6, 2025Locations: 1
Eligibility criteria

Age >18 years [+3]

Traumatic stroke [+3]