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Apnea clinical trials

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NCT ID: NCT00646971 Terminated - Oxidative Stress Clinical Trials

Oxidative Stress and Endothelial Dysfunction in Obstructive Sleep Apnea

SOREVAS
Start date: January 2008
Phase: N/A
Study type: Interventional

Patients with sleep apnea syndrome have repeated apneic events that induce periodic hypoxia-reoxygenation, drawing away an overproduction of oxidants. This exaggerated generation of oxidants is associated with a dysfunction of the vascular endothelium that evolves, in its turn, towards cardiovascular diseases such as systemic hypertension, stroke, and myocardial infarction. The major aim of our study is to examine the effect of CPAP treatment on biochemical (markers of oxidative stress) and functional (endothelium-dependent vascular relaxation reactivity) abnormalities at 1 and 4 weeks of treatment.

NCT ID: NCT00642486 Completed - Clinical trials for Sleep Apnea, Obstructive

Portable Monitoring for Diagnosis and Management of Sleep Apnea

HomePAP
Start date: February 2008
Phase: N/A
Study type: Interventional

This multi-site project compares compares the efficiency of a home-based portable monitoring strategy to a standard of care sleep laboratory-based strategy for the diagnosis and positive airway pressure treatment of obstructive sleep apnea in adults.

NCT ID: NCT00640536 Completed - Clinical trials for Sleep Apnea, Obstructive

Right Ventricular Function in Obstructive Sleep Apnea

Start date: June 2006
Phase: N/A
Study type: Observational

The purpose of this study is to determine the structural and functional cardiac alterations in obstructive sleep apne (OSA) independent from systemic and pulmonary arterial hypertension and their correlation to the severity of OSA.

NCT ID: NCT00635674 Completed - Metabolic Syndrome Clinical Trials

Effects of CPAP on Cardiovascular Risk in Obstructive Sleep Apnea (OSA) and Metabolic Syndrome

Start date: February 2007
Phase: N/A
Study type: Interventional

The increased risk of atherosclerotic morbidity and mortality in patients with obstructive sleep apnea (OSA) has been linked to arterial hypertension, insulin resistance, systemic inflammation, and oxidative stress in previous studies. We aimed to determine the effects of 8-weeks therapy with continuous positive airway pressure (CPAP) on glucose and lipid profile, systemic inflammation, oxidative stress, and the global cardiovascular disease (CVD) risk in patients with severe OSA and metabolic syndrome.

NCT ID: NCT00630474 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Nasal Decongestion and Obstructive Sleep Apnea

Start date: January 2004
Phase: Phase 4
Study type: Interventional

Whether impaired nasal breathing contributes to sleep related breathing disturbances has not been known. Therefore, the purpose of the study is to compare the effect of xylometazoline, a drug that decongests the nasal mucosa when applied locally, with placebo in terms of sleep and nocturnal breathing and daytime performance.

NCT ID: NCT00628511 Completed - Sleep Apnea Clinical Trials

Validation of Portable Monitoring Device for Diagnosing Sleep Apnea

Start date: January 2007
Phase: N/A
Study type: Observational

portable monitoring device could diagnose sleep apnea in high risk patients.

NCT ID: NCT00623246 Completed - Clinical trials for Sleep Apnea, Obstructive

Evaluating Behavioral Treatments to Improve Adherence to Continuous Positive Airway Pressure (CPAP) Therapy in People With Obstructive Sleep Apnea (The BREATHE Study)

BREATHE
Start date: December 2007
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is a serious sleep disorder in which a person repeatedly stops breathing or experiences shallow breathing for short periods of time during sleep. The most common treatment for OSA is the use of a continuous positive airway pressure (CPAP) machine, but many people have trouble adhering to the treatment schedule. This study will evaluate the effectiveness of two behavioral therapy programs used in combination with CPAP for improving treatment adherence in people with OSA.

NCT ID: NCT00620659 Terminated - Clinical trials for Sleep Apnea, Obstructive

Treatment of Refractory Excessive Daytime Sleepiness in Patients With Obstructive Sleep Apnea/Hypopnea Syndrome (OSA/HS) Using Nasal Continuous Positive Airway Pressure (nCPAP) Therapy (0249-015)

Start date: February 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of MK0249 in treating refractory excessive daytime sleepiness (EDS) in patients with Obstructive Sleep Apnea/Hypopnea Syndrome (OSA/HS) using nasal continuous positive airway pressure (nCPAP) therapy.

NCT ID: NCT00614250 Completed - Clinical trials for Sleep Apnea, Obstructive

Evaluation of the Effect of AVE0657 on Obstructive Sleep Apnea

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the activity of 4 escalating doses of AVE0657 in comparison to placebo in patients with Obstructive Sleep Apnea Hypopnea Syndrome.

NCT ID: NCT00607893 Completed - Clinical trials for Cardiovascular Diseases

Efficacy of Continuous Positive Airway Pressure in Reducing Oxidative Stress in Individuals With Sleep Apnea

SASS
Start date: September 2006
Phase: N/A
Study type: Interventional

Sleep-disordered breathing (SDB) is a condition in which a person experiences frequent breathing pauses during sleep, also known as sleep apnea. There is evidence that the recurrent sleep arousal and associated shortage of oxygen in the body may increase risk for cardiovascular disease (CVD). It is believed that treatment with continuous positive airway pressure (CPAP) may reduce certain risk factors for heart disease, including markers of inflammation and oxidative stress. This study will evaluate the effectiveness of CPAP in reducing CVD risk factors in people with SDB.