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Sleep Apnea Syndrome clinical trials

View clinical trials related to Sleep Apnea Syndrome.

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NCT ID: NCT00936273 Recruiting - Clinical trials for Sleep Apnea Syndrome

Sleep Apnea and Periodic Breathing

DLI
Start date: June 2009
Phase: N/A
Study type: Observational

The purpose of this study is to determine the double loop index (DLI) threshold with optimal sensitivity and specificity. The investigators hypothesize that the DLI gives a better reflection of the pathophysiology of the disease than the apnea-hypopnea-index (AHI).

NCT ID: NCT00885573 Completed - Clinical trials for Sleep Apnea Syndrome

Pharyngeal Sensitivity in Diagnosis Algorithm for Sleep Apnea Syndrome

SENSITEST
Start date: December 2008
Phase: N/A
Study type: Interventional

Pharyngeal sensitivity is a determinant parameter of pharyngeal functioning, particularly regarding protective dilator reflexes of upper airway. Preliminary results have suggested that the use of this parameter in diagnosis algorithm such as linear discriminant analysis and random forest could predict the presence of sleep apnea syndrome in almost 98% of patients. Our study aims at validating a new diagnosis method of sleep disordered breathing which will be compared with nocturnal polysomnography, the reference method to diagnose sleep disordered breathing. Pharyngeal sensitivity will be measured using the SENSITEST device which allows an automatic measurement of the pharyngeal sensation. The use of this parameter in diagnosis algorithm will be compared with polysomnographic results.

NCT ID: NCT00816829 Terminated - Obesity Clinical Trials

Effect of Fenofibrate on Sleep Apnea Syndrome

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Objectives: to investigate for the potential effect of fenofibrate on symptoms and biological changes associated with sleep apnea syndrome.

NCT ID: NCT00746928 Active, not recruiting - Clinical trials for Sleep Apnea Syndrome

Cardiovascular Consequences of Intermittent Hypoxia in Healthy Subjects

Start date: September 2005
Phase: N/A
Study type: Interventional

The study is a prospective field evaluation to assess the effects of the chronic Intermittent Hypoxia exposure in 12 healthy humans. Precisely, the study was designed to : Set up a new model of Chronic Intermittent Hypoxia (CIH) applied to healthy human. This CIH is mimicking the CIH undergone by patients suffering from Sleep Apnea Syndrome. Evaluate the cardiovascular effect of CIH. Neuronal and humoral sympathetic control, blood pressure control, vascular resistance. Evaluate the Sleep quality, the ventilation under exposure and the long terms effect on ventilation control of CIH (central and peripheral chemoreflex). Investigates the biological aspects of CIH exposure.

NCT ID: NCT00517777 Recruiting - Metabolic Syndrome Clinical Trials

Continuous Positive Airway Pressure in Sleep Apnea Syndrome: Effects on Metabolic Syndrome and Cardiac Damage

Start date: August 2007
Phase: Phase 4
Study type: Interventional

To assess in moderate to severe Obstructive Sleep Apnea the effects of one year therapy with nighttime continuous positive airway pressure ventilation on the prevalence of metabolic syndrome and cardiovascular damage.

NCT ID: NCT00317083 Completed - Clinical trials for Sleep Apnea Syndrome

Cough Reflex and Obstructive Sleep Apnea Syndrome

Start date: November 2001
Phase: N/A
Study type: Interventional

Up to 70% of obese patients undergoing bariatric surgery have obstructive sleep apnea syndrome (OSAS). OSAS is responsible for laryngeal sensory impairment. As the afferent neural pathway involved in the initiation of cough is located in the laryngeal epithelium, cough reflex sensitivity may be decreased in obese OSAS patients. The researchers therefore conducted this study to determine the effect of OSAS associated with obesity on cough reflex sensitivity, assessed by cough reflex threshold to an inhaled irritant (citric acid).

NCT ID: NCT00152711 Recruiting - Clinical trials for Nonalcoholic Steatohepatitis

Impact of nCPAP Treatment on Liver Function in Patients With Sleep Apnea Syndrome and Nonalcoholic Steatohepatitis

Start date: September 2004
Phase: N/A
Study type: Interventional

This study aims to evaluate the impact of nasal continuous positive airway pressure (nCPAP) treatment on liver enzymes in patients with sleep apnea syndrome and nonalcoholic steatohepatitis. Using a cross over design, the evolution of liver enzymes will be evaluated in 40 patients during a consecutive period of 6 weeks, with and without nCPAP treatment.

NCT ID: NCT00152672 Recruiting - Clinical trials for Sleep Apnea Syndrome

Treatment of Sleep Apnea Syndrome With nCPAP Versus Oral Appliance

Start date: June 2005
Phase: N/A
Study type: Interventional

This prospective randomized cross over study aims to compare nCPAP with mandibular advancement device for the treatment of sleep apnea syndrome.The effectiveness of nCPAP and oral appliance on apnea-hypopnea index, daytime sleepiness and quality of life will be compared in 60 patients.

NCT ID: NCT00001723 Completed - Obesity Clinical Trials

Safety and Efficacy of Xenical in Children and Adolescents With Obesity-Related Diseases

Start date: May 1998
Phase: Phase 2
Study type: Interventional

Obesity is a condition affecting one-third off the U.S. population and is a major risk actor for the development of Type 2 diabetes, hyperlipidemia (increased levels of fat in the blood), hypertension (high blood pressure), and other disorders of the heart and lungs. Individuals with the onset of obesity during childhood or adolescence are at an increased risk of obesity-related, diseases, both during adolescence and later in adult life. African American girls and women are at an increased risk for obesity, and have substantial rates of obesity-related diseases and causes of death. Further, many African American adult women fail to respond to many of the therapeutic approaches used to treat obesity. At present there are no medical therapies proven effective for the correction of severe obesity in children or adolescents. One medication that may have a favorable risk-benefit ratio in pediatric populations is Orlistat (Xenical, Hoffmann LaRoche). Orlistat works by preventing the action of enzymes in the digestive process, interfering with the absorption of approximately 1/3 of the fat eaten in the diet. Xenical appears to be effective for reducing weight and obesity-associated diseases in obese adults. Researchers propose to determine the safety, tolerability, and efficacy of Xenical in 12-17 year old severely obese African American and Caucasian children and adolescents who have one or more obesity-related disease (hypertension, hyperlipidemia, sleep apnea, hepatic steatosis, insulin resistance, impaired glucose tolerance, or Type 2 diabetes).