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Sleep Apnea clinical trials

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NCT ID: NCT02387476 Completed - Clinical trials for Obstructive Sleep Apnea

Non-Inferiority Study of the FRESCA Mask Versus Existing CPAP Mask for Treatment of Obstructive Sleep Apnea

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

This will be a prospective study in subjects with Obstructive Sleep Apnea (OSA) to characterize the clinical performance during a single night of therapy with a FRESCA mask compared with a single night of therapy with their existing nasal Continuous Positive Airway Pressure (CPAP) mask.

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: 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: 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: 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.

NCT ID: NCT02064114 Completed - Obesity Clinical Trials

SORT - AF Supervised Obesity Reduction Trial for AF Ablation Patients

SORT-AF
Start date: January 2014
Phase: N/A
Study type: Interventional

Study hypothesis: Weight reduction in obese patients with atrial fibrillation. Obese patients benefit from an obesity treatment after atrial fibrillation ablation. Study design: A prospective randomized, open-label clinical trial.

NCT ID: NCT02045173 Completed - Sleep Apnea Clinical Trials

Automate Detection of Sleep Apnea by ApneascanTM

AIRLESS
Start date: January 2014
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare, three months after implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy-defibrillator (CRT-D), the apnea-hypopnea index (AHI) obtained from conventional in-lab NPSG/NPG (AHIPSG) with similar indices obtained from autoscoring algorithms of the ApneaScan™, an implantable impedance-based respiration sensor (AHIAS).