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Sleep Apnea clinical trials

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NCT ID: NCT02296710 Completed - Sleep Apnea Clinical Trials

Echocardiographic Parameter and Sleep Apnea Changes After Mitral Valve Surgery

MitralHDZ
Start date: August 2014
Phase: N/A
Study type: Interventional

The investigators evaluate the changes of echocardiographic and sleep apnea parameters after mitral valve surgery. The patients undergo echocardiographic and sleep apnea control before surgery. After a period of 3-5 months, they undergo a second echocardiographic and sleep apnea control and the results are evaluated.

NCT ID: NCT02295202 Completed - Metabolic Syndrome Clinical Trials

Impact of Obstructive Sleep Apnea Treatment in Patients With Metabolic Syndrome

TREATOSA-MS
Start date: March 2015
Phase: Phase 4
Study type: Interventional

Obstructive Sleep Apnea (OSA) is a common condition that may induce hemodynamic and metabolic dysregulation. However, it is not clear if OSA is a mere epiphenomenon or contributes to increase the morbidity associated with metabolic syndrome. This study was designed to evaluate the impact of OSA treatment with CPAP in consecutive patients with metabolic syndrome.

NCT ID: NCT02279056 Completed - Insomnia Clinical Trials

Randomized Controlled Trial of a Self-help Book for Insomnia in Patients With Co-morbid OSA and Insomnia

Start date: October 2014
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is a common sleep disorder treated with continuous positive airway pressure (CPAP). Some OSA patients also suffer from co-morbid insomnia. CPAP treatment may be complicated in patients with co-morbid insomnia. This project evaluates the effects of a self-help book for insomnia in patients being treated with CPAP for OSA.

NCT ID: NCT02265133 Active, not recruiting - Sleep Apnea Clinical Trials

Corneal Sensitivity in Patients With Sleep Apnea Syndrome

Start date: July 17, 2015
Phase:
Study type: Observational

This study is a prospective, single center clinical trial to assess corneal sensitivity and nerve fiber morphology in patients with sleep apnea compared to normal controls. Healthy volunteers with no history of ocular or uncontrollable systemic disease will be encouraged to participate in the study. After execution and review of the consenting procedures, a detailed history will be taken and a slit lamp examination performed, verifying ocular health. This consists of an examination of both eyes including assessments of ocular lids, lashes, cornea and conjunctival evaluation. Corneal touch thresholds will be tested with a Cochet-Bonnet aesthesiometer, a standard non-invasive measure of corneal sensitivity. Corneal nerves will be imaged using a modified HRT in vivo confocal microscope. The in vivo confocal microscope allows for high resolution imaging of the nerve plexus under the corneal epithelium. This corneal nerve plexus is responsible for corneal sensitively and changes or loss have been established as an early, sensitive indicator of corneal neuropathy. The investigators anticipate that this study will require approximately 30 patients for each group and will last approximately 12 months for recruitment and completion of subject visit phases. There is only one clinical visit designed for this project, unscheduled visits may be scheduled in case of an adverse event. Patient recruitment will be complete at the one-year time point. At the 14 month time point, all data points will have been collected and assessment of the outcome measure (corneal sensitivity in sleep apnea patients versus control patients) will be complete.

NCT ID: NCT02213159 Completed - Obesity Clinical Trials

Dexmedetomidine for Postoperative Analgesia After Bariatric Surgery

Start date: July 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if Dexmedetomidine given at the end of surgery will reduce postoperative morphine consumption and improve postoperative quality of recovery as compared to morphine in patients undergoing laparoscopic bariatric surgery.

NCT ID: NCT02188498 Completed - Sleep Apnea Clinical Trials

Electrocardiography Data Analysis in Sleep Disorders

Holter
Start date: September 2013
Phase:
Study type: Observational

The objective of this study is to determine if a non-invasive technique, using an innovative analysis of electrocardiogram (ECG) data, would allow for detection of respiratory events during sleep and discrimination between central and obstructive apnea. Obstructive Sleep Apnea (OSA) is the most common respiratory disturbance seen during sleep, with an estimated prevalence of 10 % in the population and is strongly associated with the development of cardiovascular disease. In patients with underlying cardiac disease, particularly in heart failure (HF), central respiratory events such as Cheyne-Stokes Respiration (CSR) are often seen during sleep. The presence of CSR is also associated with increased cardiovascular morbidity and mortality. Currently, the identification and classification of sleep related respiratory disturbances is performed during over-night sleep studies (polysomnography), which are labor-intensive, time-consuming, expensive and difficult for patients. Thus, the development of alternative techniques to assist in the identification of those events in the outpatient setting is of marked importance for widespread screening of sleep apnea.

NCT ID: NCT02159664 Terminated - Sleep Apnea Clinical Trials

Influence of Didgeridoo Practice on UA Obstruction Levels in Moderate OSA

Start date: December 2014
Phase: N/A
Study type: Interventional

Didgeridoo practice has been shown to improve OSA severity. The aim of our study is to assess the changes in upper airways obstruction levels before and after Didgeridoo practice in moderate OSA patients.

NCT ID: NCT02148991 Completed - Hypertension Clinical Trials

Clinical Trial in Patients With Hypertension and Left Ventricular Dysfunction

Start date: July 2014
Phase: N/A
Study type: Observational

Arterial hypertension causes adverse effects on the entire cardiovascular system, with effects centrally such as diastolic dysfunction and structural changes of the left ventricle and, peripherally such as endothelial dysfunction and increased thickness of the vessels. Co-existing diseases, such as diabetes mellitus, renal dysfunction, sleep apnea, etc. further aggravate the prognosis of these patients. In addition the rate of patients aged > 65 years suffering from un-diagnosed or diagnosed arterial hypertension was 78% for women and 64% for male patients. This population consists from elderly or very elderly patients (over 65 and 80 years respectively) who exhibit more comorbidities and probably less compliance with antihypertensive therapy. Finally, at every age the disease and its effects can affect the quality of life of patients. The main purpose of this study is to investigate the efficacy of antihypertensive therapy (irbesartan alone or in combination with amplodipine and carvedilol) on the cardiovascular system (diastolic left ventricular function, the function of the endothelium (FMD) and the thickness of the common carotid artery). The secondary objective of the study is to monitor the quality of life (Quality of Life - QoL) of patients. Additionally the investigators will seek the correlation of results with co-morbidities, compliance, and patient age.

NCT ID: NCT02131610 Recruiting - Sleep Apnea Clinical Trials

Epigenetics Modifications in Obstructive Sleep Apnea

EPIOSA
Start date: March 2013
Phase: N/A
Study type: Observational [Patient Registry]

Changes in epigenetic regulation of genes involved in systemic inflammation and metabolic dysfunction in OSA are linked with accelerated cardiovascular morbidity.

NCT ID: NCT02108197 Completed - Clinical trials for Gestational Diabetes

Sleep Apnea and Gestational Diabetes

Start date: April 2014
Phase: N/A
Study type: Interventional

The investigators hypothesize that pregnant women with gestational diabetes will have a high incidence of sleep apnea, and that the treatment of sleep apnea will lead to improved glucose control in these women.