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Apnea clinical trials

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NCT ID: NCT01141829 Recruiting - Oxidative Stress Clinical Trials

NADPH Oxidase Polymorphisms in Obstructive Sleep Apnea Syndrome (OSAS)

Start date: n/a
Phase: N/A
Study type: Observational

Obstructive Sleep Apnea (OSA) is associated with increased oxidative stress. The major sources of Reactive Oxygen Species (ROS) in the vasculature are the NADPH oxidases. Several polymorphisms related to NADPH oxidase expression or NADPH oxidase activity has been identified. The investigators are going to compare the distribution of the allelic frequencies of A-930G and C242T polymorphisms and their possible relationship with the levels of 8-isoprostanes as a marker of oxidative stress in patients with OSA and in a control group without OSA.

NCT ID: NCT01137214 Withdrawn - Sleep Apnea Clinical Trials

Outcome and Treatment of Complex Sleep Apnea

Start date: June 2011
Phase: Phase 2
Study type: Interventional

The purpose of the project is: 1. to determine the incidence of complex sleep apnea 2. to determine what percentage of cases will resolve over time with therapy with Continuous Positive Airway Pressure 3. Determine whether there is any difference in outcome, in those with persistent complex sleep apnea on CPAP, between those treated with CPAP or adaptive servo-ventilation.

NCT ID: NCT01135303 Completed - Clinical trials for Sleep Apnea Syndromes

Effectiveness of VistaO2 Device in Screening of Sleep Apnea/Hypopnea Syndrome

VISTAO2
Start date: February 2009
Phase: N/A
Study type: Interventional

The high prevalence (9% in men and 4% in women) of sleep apnea / hypopnea syndrome (SAHS) in adults is now well documented as well as its cardiovascular repercussions. Previous studies showed a conclusive link between SAHS and severe cardiovascular diseases such as hypertension, myocardial infarction, heart failure and stroke.Then, SAHS is a public health issue in adults. In this context, early detection of such a disease is crucial if the management is tailored to the patient, the practitioner's choice of therapy moving towards continuous positive airway pressure (CPAP) or mandibular advancement device. The detection is based on full nocturnal polysomnography or polygraphic recordings. Polysomnography remains the gold standard but it is a time consuming and costly examination. Polygraphic recording is a test that allows simplified the diagnosis of severe patients, but may not be sufficient for mild form of SAHS. Thus, the SAHS is a pathology under-diagnosed and under-treated. The validation of a technique for identifying patients most at risk to either limit the number of polysomnographic examination is requested.

NCT ID: NCT01128816 Terminated - Heart Failure Clinical Trials

Effect of Adaptive Servo Ventilation (ASV) on Survival and Hospital Admissions in Heart Failure

ADVENT-HF
Start date: May 2010
Phase: N/A
Study type: Interventional

Sleep Apnea (SA) is a disorder that causes pauses in breathing during sleep that expose the heart to oxygen deprivation. It is common in patients with heart failure (HF) where it is associated with increased risk of hospitalizations and death. It is not known however whether treating SA reduces these risks. This study is looking at whether a respiratory device known as Adaptive Servo Ventilation (ASV) can reduce the rate of cardiovascular hospitalizations and death in subjects with HF and SA. Study subjects will randomly receive either their regular medications OR their regular medications plus ASV. They will be followed for approximately 5 years and information relevant to their health will be collected and compared.

NCT ID: NCT01124370 Completed - Sleep Apnea Clinical Trials

Chronic Evaluation of Respicardia Therapy

Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the chronic safety and efficacy of phrenic nerve stimulation on central sleep apnea (CSA). Clinically, CSA events translate into sleep fragmentation, excessive daytime sleepiness, reduced exercise capacity, and possibly ventricular arrhythmias. The study is chronic in nature, such that subjects will undergo the implantation of an implantable pulse generator and stimulation lead. A sensing lead may also be placed during the initial implant procedure. Subjects will be followed for up to six-months on therapy to assess respiratory and heart failure outcomes. Following the six-month therapy visit, subjects will enter into a long-term follow-up phase until the completion of the study. It is anticipated that data obtained in this study will show that the proposed intervention can modify respiration with a low incidence of adverse effects. The results of this trial are intended to be used to develop a subsequent protocol for pivotal study.

NCT ID: NCT01117974 Withdrawn - Clinical trials for Obstructive Sleep Apnea

Neck Liposuction for the Treatment of Obstructive Sleep Apnea

Start date: n/a
Phase: N/A
Study type: Interventional

Liposuction, one of the most common cosmetic procedures performed in the United States, is a surgical technique used to reduce localized areas of excess subcutaneous fat. The neck is a common area of treatment, where liposuction reduces fat volume and neck size. We hypothesize that suctioned removal of fat of the neck will reduce the severity of obstructive sleep apnea.

NCT ID: NCT01117064 Completed - Clinical trials for Obstructive Sleep Apnea

Neuromodulation Therapy Device for the Treatment of Sleep Apnea

Start date: February 2010
Phase: Phase 1
Study type: Interventional

We are looking to test a novel device in the treatment of Obstructive Sleep Apnea (OSA). Rather than using positive pressure to open the airways, we are testing a device that delivers an auditory tone to affect neuromodulation. We will test its efficacy in treating OSA while minimizing sleep disturbance. As this device is much less cumbersome to wear, we hope this therapy device will also improve compliance with treatment.

NCT ID: NCT01116375 Completed - Obesity Clinical Trials

Does Treating Obstructive Sleep Apnea in Obese Canadian Youth Improve Blood Sugar Control?

IMPACT Obesity
Start date: June 2010
Phase: N/A
Study type: Observational

To determine whether, in obese children with moderate-severe Obstructive Sleep Apnea who are prescribed Positive Airway Pressure(PAP) therapy, increased hours of PAP usage per night over a one-year period is associated with a greater improvement in HOMA-IR

NCT ID: NCT01115686 Withdrawn - Sleep Apnea Clinical Trials

Branched-chain Aminoacids in Sleep Apnea Syndromes (ARSAS)

ARSAS
Start date: June 2010
Phase: Phase 3
Study type: Interventional

The initial hypothesis is that branched-chain aminoacids (BCAA) administration could be beneficial to patients suffering from sleep apnea syndrome (SAS), the aim of the present work is to verify this hypothesis. The literature data demonstrate that a BCAA complementation improves the physical performances, protects lean mass and increases VO2 max during training. We demonstrated earlier that this complementation can cure at less partly the hypoxemia of chronic obstructive pulmonary patients by a stimulation of respiratory centres.

NCT ID: NCT01108081 Completed - Sleep Apnea Clinical Trials

Telemedicine Interventions for Obstructive Sleep Apnea (OSA)

Start date: October 2010
Phase: Phase 3
Study type: Interventional

This project is investigating whether both moderate-intensity physical activity and dietary weight loss will independently reduce sleep apnea symptoms and improve quality of life.