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Sleep Apnea, Obstructive clinical trials

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NCT ID: NCT01195064 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Endothelial Function Study Before Cardiovascular Surgery

COPD-OSAS
Start date: April 2010
Phase:
Study type: Observational

The aim of this clinical trial is to evaluate the effect of chronic obstructive pulmonary disease (COPD) and/or obstructive sleep apnea syndrome (OSAS) on the endothelial function, before cardiovascular surgery, compared to non COPD non OSAS patients undergoing also a cardiovascular surgery, by an observational physiological study. An interim analysis will be performed when 100 patients will be included.

NCT ID: NCT01136122 Terminated - Clinical trials for Obstructive Sleep Apnea

Effects of PAP Treatment of OSA in Patients With Heart Failure

OSA-MRI
Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to see if treatment of OSA with the CPAP device makes a difference to insulin resistance and heart disease.

NCT ID: NCT01107795 Terminated - Clinical trials for Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS)

Prospective Study to Evaluate Outcomes From Transoral BOT Resection for OSAHS

Start date: March 4, 2010
Phase:
Study type: Observational

This is a prospective observational study that will collect outcome data for patients who choose to undergo transoral tongue base operations for Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS)as part of their standard of care treatment. This is a data collection study only and does not provide for evaluations or treatment of OSAHS.

NCT ID: NCT01089257 Terminated - Clinical trials for Obstructive Sleep Apnea Syndrome

Cardiovascular Impairments and Obstructive Sleep Apnea Syndrome

INFRASAS
Start date: November 2007
Phase:
Study type: Observational

Which are the anthropometric parameters and/or of severity of the syndrome of apnea of sleep (SAS) which make it possible to anticipate occurred of vascular anomalies, anatomical and/or functional precociously found among patients SAS? Secondary objectives: 1. Which are the anthropometric parameters and/or of severity of SAS allowing to anticipate occurred of early of the cardiac function and/or rhythmic anomalies found among patients SAS? 2. Do there exist biological markers who allow to anticipate the early vascular lesions or the anomalies beginners of the cardiac function? 3. Which are the cardiovascular effects of a treatment of SAS by Continuous Positive Pressure (PC) after 3 to 6 months of treatment? 4. Do the identified early cardiovascular attacks and/or the biological anomalies make it possible to predict occurred of cardiovascular events in this population of patients carrying SAS (followed longitudinal at 5 years)?

NCT ID: NCT01051297 Terminated - Clinical trials for Obstructive Sleep Apnea

Obstructive Sleep Apnea and Venous Thromboembolism

OSAVTE
Start date: March 2009
Phase: N/A
Study type: Observational

There is a clear link between obstructive sleep apnea (OSA) and cardiovascular disease. However, there has been no clear link between OSA and venous thromboembolism (VTE). The objective of this study is to evaluate such a link.

NCT ID: NCT01027806 Terminated - Clinical trials for Obstructive Sleep Apnea

Effect of Montelukast Therapy in Obstructive Sleep Apnea(OSA) Children

32543
Start date: July 2010
Phase: Phase 4
Study type: Interventional

The investigators leading hypotheses are: - Oral therapy with montelukast may lead to improved sleep study findings in children with mild to moderate Obstructive Sleep Apnea Syndrome (OSAS) who require surgical removal of adenoids and tonsils for OSAS. - A significant proportion of the children with OSAS treated with montelukast will show reduced severity of OSAS, and this will remove the need for surgical intervention.

NCT ID: NCT01027078 Terminated - Clinical trials for Obstructive Sleep Apnea

Mechanism of Endothelial Dysfunction in Obstructive Sleep Apnea (OSA)

Start date: November 2009
Phase:
Study type: Observational

The investigators hypothesized that patients with Obstructive Sleep Apnea (OSA) who are free of any cardiovascular disease will have early microcirculatory changes that are unique to OSA, and therefore would resolve with treatment of OSA.

NCT ID: NCT01026207 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Portable Monitoring Device for the Diagnosis of Sleep Apnea in Patients With Chronic Obstructive Pulmonary Disease

Start date: August 2009
Phase: N/A
Study type: Observational

Introduction: The prevalence of overlap between Chronic Obstructive Pulmonary Disease (COPD) and Obstructive Sleep Apnea Syndrome (OSAS) is around 10%. This overlap syndrome is an important issue because is related to nocturnal desaturation and its complications. The use of portable monitoring devices (PM) for the diagnosis of OSAS was recently accepted as an alternative to full-night polysomnography (PSG). However, there are not studies evaluating the PM recording in COPD patients to detect or exclude OSAS. Objective: To evaluate if a PM (Stardust®, Respironics, Inc, USA) could accurately measure the apnea-hypopnea index (AHI) in COPD patients with a suspicion of OSAS.

NCT ID: NCT00952211 Terminated - Stroke Clinical Trials

Burden of Obstructive Sleep Apnea in Stroke (BOSAST)

BOSAST
Start date: August 2009
Phase: Phase 4
Study type: Interventional

There are two purposes of this study. The first purpose is to define the frequency of obstructive sleep apnea in stroke survivors as well as its association with fatigue and quality of life. The second purpose is to determine if continuous positive airways pressure (CPAP) treatment can have a beneficial effect on these patients' fatigue and quality of life.

NCT ID: NCT00942643 Terminated - Clinical trials for Obstructive Sleep Apnea

Endothelial Damage and Atherosclerosis in Obstructive Sleep Apnea

Start date: May 2008
Phase: N/A
Study type: Interventional

The investigators hypothesize that obstructive sleep apnea (OSA) may lead to increased formation/accumulation of advanced glycation ends (AGEs), and that the increase in AGEs is contributed in part by increased insulin resistance. The investigators further hypothesize that AGEs contribute to vascular endothelial damage and ultimately atherosclerosis in OSA. The objectives of this study are: 1. To explore the relationship between insulin resistance and AGEs in OSA 2. To study the relationship between AGE and vascular endothelial dysfunction in OSA 3. To study the relationship between AGE and early atherosclerosis in OSA