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Apnea clinical trials

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NCT ID: NCT03958396 Completed - Clinical trials for Obstructive Sleep Apnea

Remifentanil in Children With Obstructive Sleep Apnea

ROSA
Start date: September 1, 2015
Phase: Early Phase 1
Study type: Interventional

This investigation tested the hypothesis that children with obstructive sleep apnea have an increased pharmacodynamic sensitivity to the miotic and respiratory depressant effects of the prototypic μ-opioid agonist remifentanil.

NCT ID: NCT03955120 Completed - Insomnia Clinical Trials

Validation of the Dayzz Digital Sleep Training App in Insomnia and Sleep Apnea

Start date: January 29, 2019
Phase: N/A
Study type: Interventional

The prevalence of sleep disorders has achieved epidemic proportions in Western countries. Despite this, assessment and treatment of sleep disorders remains infrequent, unattainable, and often costly. Dayzz is aware of the need for easily accessible, user-friendly, and affordable treatment strategies for known sleep conditions. This research proposes a randomized controlled outcome study aimed to validate a, digitized, cost-effective mobile app which assesses and manages insomnia and CPAP adherence in persons with sleep apnea. The app's sleep training protocols recommend life-style and behavioral changes and tracks these changes with the aim of improving sleep and well-being. In this study, the dayzz app digital treatment protocol will be compared to the standard treatment for these sleep conditions by a sleep professional.

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: 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: 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.

NCT ID: NCT03869125 Completed - Clinical trials for Obstructive Sleep Apnea

Masked Hypertension in Patients With Obstructive Sleep Apnoea

Start date: March 22, 2019
Phase:
Study type: Observational

Assessment of the possible difference in masked hypertension prevalence when it is evaluated by automated office blood pressure measurement (AOBPM) instead of office blood pressure measurement (OBPM) in patients with obstructive sleep apnoea.

NCT ID: NCT03857191 Completed - Clinical trials for Sleep Apnea, Obstructive

Nutritional Rehabilitation and Sleep Apnea in the Obese

DIETSLEEP
Start date: March 22, 2019
Phase:
Study type: Observational

In obese patients, the prevalence of obstructive sleep apnea (OSA) is around 40% in men and 30% in women. Weight loss after bariatric surgery significantly improves OSA, with 75% of patients having a reduction in OSA severity or becoming non-apneic. We hypothesize a similar effect on OSA of nutritional and psychocomportemental rehabilitation for obese patients. However, we expect weight loss and blood pressure reduction to probably be lower in obese patients who have OSA and nutritional rehabilitation alone than in those who are treated for their OSA or are without OSA. To address this question, we will conduct an observational study on obese patients, treated or not for OSA, following nutritional and psychocomportemental rehabilitation.