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Sleep Apnea, Obstructive clinical trials

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NCT ID: NCT03940781 Completed - Clinical trials for Obstructive Sleep Apnea of Adult

Effects of Rehabilitation for Patients With Obstructive Sleep Apnea

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

In previous review study, it was hypothesized that a comprehensive rehabilitation can combine both local pharyngeal muscle exercise and systemic cardiopulmonary rehabilitation for the OSA patients with oropharyngeal muscle dysfunction or ventilator drive instability. To develop a comprehensive rehabilitation model is of innovative care strategy in this study.

NCT ID: NCT03938259 Completed - Clinical trials for Obstructive Sleep Apnea

Effect of Opioids on Ventilation in Children With Obstructive Sleep Apnea

Start date: July 1, 2019
Phase:
Study type: Observational [Patient Registry]

The sole objective in this study is to evaluate if routine amounts of opioids given for tonsillectomy in children have greater amounts of respiratory depression in children with documented obstructive sleep apnea when compared with patients that do not have obstructive sleep apnea

NCT ID: NCT03933800 Completed - Clinical trials for Obstructive Sleep Apnea

High Flow Nasal Cannula Therapy for Childhood OSA

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The main objective of this study is to evaluate the efficacy of high-flow nasal cannula (HFNC) therapy in children with OSA. Children and adolescents aged 6 to 18 years old with a diagnosis of moderate-to-severe OSA requiring CPAP therapy will be recruited. In phase 1 study, eligible subject will be recruited for HFNC therapy titration with PSG to assess treatment efficacy. After titration, if HFNC therapy is shown to be effective, the participants will be recruited into the phase 2 intervention period to evaluate the compliance and quality of life with HFNC therapy. At baseline and follow-up visits, neurobehavioural and quality of life surveys will be completed, compliance data will be obtained.

NCT ID: NCT03930875 Completed - Clinical trials for Obstructive Sleep Apnea

Aspirin Resistance in OSA Patients

Start date: December 12, 2017
Phase:
Study type: Observational

Obstructive Sleep Apnea (OSA) patients are at increased risk of major cardiovascular events, so many patients take aspirin for prevention. Poor responsiveness to aspirin is a major clinical concern because it can potentially worsen the prognosis of OSA patients. However, continuous positive airway pressure (CPAP) therapy that is considered standard of care for OSA treatment may potentially lead to improvement in responsiveness to aspirin. This study will determine whether CPAP therapy decreases patients' aspirin resistance in OSA patients with a new diagnosis or existing moderate to severe OSA who are treated with CPAP and take aspirin for prevention.

NCT ID: NCT03930563 Completed - Clinical trials for Obstructive Sleep Apnea

Inorganic Nitrate and OSA

Start date: June 12, 2019
Phase: N/A
Study type: Interventional

The main purpose of this study is to determine if acute beetroot juice supplementation reduces peripheral chemoreflex sensitivity in patients with obstructive sleep apnea. All subjects will consume low-dose (BRL), higher-dose (BRH), and placebo (BRP) beetroot juice randomly on three independent study visits. Beetroot juice also improves blood flow thus, the investigators will also measure blood flow to the carotid chemoreceptors.

NCT ID: NCT03926832 Completed - Fatigue Clinical Trials

Prevalence of Obstructive Sleep Apnea Syndrome in Sarcoidosis and Impact of CPAP Treatment on Associated Fatigue Status

SARCOIDOSAS
Start date: April 27, 2019
Phase: N/A
Study type: Interventional

Sarcoidosis is a multisystemic granulomatous disease that affects individuals worldwide without known pathogenesis, and the role of comorbidities has not been fully assessed in the scientific literature. An increased incidence of Obstructive Sleep Apnea Syndrome (OSAS) has been described in Sarcoidosis although this association has not been explained yet and no data is available about the effect of treatment with Continuous Positive Airway Pressure (CPAP) in Sarcoidosis. Also, patients affected by Sarcoidosis usually experience a state of physical and mental weariness called fatigue and reported in approximately 60-80% sarcoid patients and thought to be a consequence of inflammatory mediators but the high prevalence of OSAS could be a remarkable bias in clinical evaluation because fatigue is also strongly associated with sleep disorders. Thus, there is a real need for assessing not only the real prevalence of OSAS in Sarcoidosis but also the effect of CPAP treatment on fatigue status experienced by sarcoidotic patients.

NCT ID: NCT03913494 Completed - Sleep Clinical Trials

Transoral Daytime Neuromuscular Electrical Stimulation in Patients With Simple Snoring

SnooZeal-snore
Start date: July 30, 2019
Phase: N/A
Study type: Interventional

Sleep Disordered Breathing (SDB) is a spectrum of conditions spanning from Simple Snoring to Severe Sleep apnea. SDB has multiple underlying mechanisms. Some portion of patients have issues with upper airway dilator muscle control; and such patients may be amenable to upper airway muscle training exercises using neuromuscular stimulation techniques. The investigators and others have published on the topic of neuromyopathy in the upper airway, defining a subgroup of OSA patients who may be amenable to training exercises. Based on this background, the investigators seek to test the hypothesis that upper airway tongue muscle training using transoral surface neuromuscular electrical stimulation may have benefits to patients with Simple Snoring.

NCT ID: NCT03899519 Completed - Clinical trials for Obstructive Sleep Apnea

Airway Ultrasonography Measurements With Cormack Lehane Classification in Patients With OSA

Start date: May 1, 2017
Phase:
Study type: Observational

Airway assessment using ultrasonography can provide an additional information in identifying difficult intubation in OSA patients. The main purpose of this study is to find the correlation of the ultrasound parameters and the Cormack Lehane Score (CL Score) as well as to identify the cut-off point of the ultrasound parameters that would differentiate between the easy and difficult intubation.

NCT ID: NCT03892772 Completed - Sleep Apnea Clinical Trials

Combination Pharmacological Interventions for Multiple Mechanisms of Obstructive Sleep Apnea

ComboPlus
Start date: January 14, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Currently, there is no pharmacological intervention for OSA that targets multiple pathophysiological deficits in combination. Here the investigators study the effect on sleep apnea severity of combinations of pharmacological agents that stimulate the pharyngeal muscles, stabilize ventilatory control, and increase the arousal threshold.

NCT ID: NCT03882801 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

Safety and Tolerability of Gefapixant (MK-7264) in Participants With Obstructive Sleep Apnea (MK-7264-039)

Start date: April 10, 2019
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the safety and tolerability of multiple dose administration of gefapixant (MK-7264) in participants with moderate to severe obstructive sleep apnea (OSA). The primary hypothesis is that multiple dose administration of gefapixant (MK-7264) in participants with moderate to severe OSA reduces the Apnea Hypopnea Index (AHI) relative to placebo.