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Apnea clinical trials

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NCT ID: NCT01349205 Terminated - Clinical trials for Obstructive Sleep Apnea

Caffeine in Children With Obstructive Sleep Apnea, Dose Response Study

Start date: March 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate whether a smaller dose of caffeine sodium benzoate 10 mg/kg IV is as effective as 20 mg/kg IV in decreasing the number of children who develop post extubation adverse upper airway respiratory events compared to placebo.

NCT ID: NCT01226641 Terminated - Clinical trials for Sleep Apnea, Obstructive

Usefulness of a Telemedicine System for OSA Patients Follow-up With High Cardiovascular Risk

TELESAS
Start date: July 2009
Phase: N/A
Study type: Interventional

The aim of this study is to determine the usefulness of a telemedicine system for the follow-up of OSA patients with a high cardiovascular risk. Our hypothesis is that the telemedicine system will enhance compliance and thus reduce self-measured blood pressure.

NCT ID: NCT01196845 Terminated - Clinical trials for Sleep Apnea Syndrome

Inflammation and Oxidative Stress of Adipose Tissue in Sleep Apnea Syndrome

ADISAS
Start date: October 16, 2010
Phase: N/A
Study type: Interventional

The main objective of this study is to evaluate the decrease of inflammation of adipose tissue in obese and non-obese patients having a sleep apnea syndrome and treated or not by continuous positive airway pressure (cPAP). An interim analysis will be performed when 40 patients will be included.

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: 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.