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Apnea clinical trials

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NCT ID: NCT02709941 Completed - Clinical trials for Obstructive Sleep Apnea

Inspiratory Muscle Strength Training for Sleep-related Breathing Disorders

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of the current study is to investigate the effects of a novel breathing training, called inspiratory muscle strength training (IMST), on sleep patterns, breathing and blood pressure for patients diagnosed with mild, moderate and severe sleep apnea.

NCT ID: NCT02701504 Completed - Sleep Apnea Clinical Trials

Undiagnosed Sleep Apnea and Bypass OperaTion

SABOT
Start date: October 1, 2013
Phase:
Study type: Observational

Sleep apnea is a prevalent disorder in patients with coronary artery disease. Previous studies suggested sleep apnea was associated with coronary plaque burden and future adverse cardiovascular events after percutaneous coronary intervention. In the SABOT study, the investigators used a FDA-approved portable sleep device to diagnose sleep apnea, and evaluate the relationship between sleep apnea and cardiovascular outcomes after non-urgent coronary artery bypass surgery.

NCT ID: NCT02683616 Completed - Clinical trials for Obstructive Sleep Apnea

Fatty Acid Metabolism in Obstructive Sleep Apnea (FAMOSA)

FAMOSA
Start date: April 1, 2015
Phase: N/A
Study type: Interventional

Obstructive sleep apnea syndrome (OSA) is a disease affecting 5-15% of population and 50-80% of type 2 diabetes mellitus (T2DM) and obese subjects. OSA causally contributes to the development of glucose intolerance and T2DM. The project is targeting the gap in providing effective treatment of metabolic impairments associated with OSA, particularly T2DM. In contrast to proved benefits of OSA treatment with CPAP (continuous positive airway pressure) on cardiovascular morbidity/mortality, studies on the impact of CPAP on diabetes control are disappointing. In fact, OSA-induced metabolic impairments might not be reversible with CPAP treatment, as investigators suggested recently. Clearly, the search for additional treatments, probably pharmacological, is warranted. Investigators hypothesize that elevated levels of free fatty acids (FFA), as detected in OSA patients, are linking OSA with the T2DM development. The aim of the study is to target adipose tissue and muscle dysfunction leading to elevated FFA and develop thus novel pharmacological treatments based on lipolysis inhibition and stimulation of FFA oxidation.

NCT ID: NCT02677584 Completed - Apnea Clinical Trials

Prophylactic Versus Therapeutic Caffeine for Apnea of Prematurity

Start date: March 2015
Phase: N/A
Study type: Interventional

Investigators hypothesized that the timing of caffeine administration in either prophylaxis or treatment of apnea of prematurity will affect the apnea response to caffeine

NCT ID: NCT02677168 Completed - Clinical trials for Sleep Apnea, Obstructive

cNEP for the Treatment of Obstructive Sleep Apnea

cNEP
Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether cNEP (continuous positive external pressure) is effective in treating obstructive sleep apnea

NCT ID: NCT02666781 Completed - Clinical trials for Obstructive Sleep Apnea

Postoperative Rostral Fluid Shift and Obstructive Sleep Apnea

Start date: April 22, 2016
Phase:
Study type: Observational

Patients with obstructive sleep apnea (OSA) are more likely to experience postoperative complications and impact significantly on healthcare resources. In the surgical population, the type and volume of IV fluid administration may contribute to the worsening of postoperative sleep apnea but the pathophysiological mechanisms have not been elucidated. Recent research from general population suggests that intravenous (IV) fluid administration worsens the severity of OSA by shifting of fluid from the legs to the neck thus increasing neck size and causing airway collapse. In this novel study, our objective is to examine the contribution of IV fluid administration and rostral fluid shift from the legs to the neck thereby leading to worsening of sleep apnea following surgery. In this prospective observational cohort study, 25 consecutive adult patients, requiring at least 2 days hospital stay, will be recruited. Following informed consent, patients will undergo portable home sleep study to determine the preoperative severity of sleep-disordered breathing. On the day of surgery, leg, neck and total body fluid volumes will be recorded, and patients will undergo general anesthetic. The results of this study will be used to design future clinical trials evaluating methods to decrease postoperative OSA worsening, as well as decreasing OSA-related postoperative complications.

NCT ID: NCT02657304 Completed - Clinical trials for Sleep Apnea Syndrome

Effect of Early Education on the Observance of CPAP Treatment

CoachSAS
Start date: March 21, 2016
Phase: N/A
Study type: Interventional

Sleep apnea (SA) affects more than 4% from general population and is largely underdiagnosed. SA can increase the occurrence of cardiovascular, endocrine and metabolic events (particularly stroke, diabetes & obesity). CPAP is currently the Gold Standard treatment of SA and to prevent these events, with a major clinical benefit, long term adherence to CPAP is a significant problem where a significant rate of rejection and abundance after 6 months of treatment.

NCT ID: NCT02643381 Completed - Clinical trials for Cardiopulmonary Arrest

Etomidate Versus Ketamine for Emergency Endotracheal Intubation: a Prospective Randomized Clinical Trial

EvK
Start date: June 6, 2016
Phase: Phase 4
Study type: Interventional

Patients who are having problems breathing sometimes require placement of a breathing tube in their mouth and windpipe. The purpose of this breathing tube is to save the patient's life. It is common to give the patient a medication to sedate him or her before the breathing tube is placed. For patients who are gravely ill two medications are commonly used: etomidate or ketamine. Both medications have risks and benefits. Researchers at UT-Southwestern Medical Center and Parkland Memorial Hospital would like to do a study to figure out which one is better for our patients.

NCT ID: NCT02627001 Completed - Apnea Clinical Trials

Nu-Mask Intraoral Airway Device Versus Conventional Bag Valve Mask Ventilation Crossover Trial

Start date: September 2014
Phase: Phase 4
Study type: Interventional

This study comprised a randomized cross-over trial of ventilation using the NuMask Intraoral Mask versus conventional Bag Valve Mask in a cadaver model among United States Army combat medics.

NCT ID: NCT02623088 Completed - Clinical trials for Obstructive Sleep Apnea

CPAP Effect on Vascular Function in Obstructive Sleep Apnea

VNI-SOH2
Start date: April 2015
Phase: N/A
Study type: Observational

Obstructive sleep apnea syndrome is responsible of endothelial dysfunction, which is a independent cardio-vascular risk factor. Assessment of pulse wave velocity (PWV) and peripheral arterial tone (PAT) are study measurements of arterial stiffness, and are strong predictors of late cardiovascular events. This study will compare long term evolution in arterial stiffness (PWV) and endothelial dysfunction (PAT) for patients treated by Positive Airway Pressure Therapies.