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Sleep Apnea, Obstructive clinical trials

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NCT ID: NCT01532050 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

PROMAD: Predicting Therapeutic Outcome of Mandibular Advancement Device Treatment in Obstructive Sleep Apnea

PROMAD
Start date: February 2012
Phase: Phase 4
Study type: Interventional

The present research intends to focus clinically on selecting the right type of patient for mandibular advancement devices (MAD) therapy using screening tools such as advanced imaging and computational methods based on CT-Scan images as well as drug-induced sleep nasendoscopy techniques with simulation of the mandibular repositioning. The core of the research project relies on known and established methods accepted in several neighboring fields, but aims at the transfer of this knowledge by integrating it into this new domain. Doing so, the proposed biomedical research is directed towards clinical applications that incorporate innovative developments on the level of the diagnosis and therapy of a specific disease, being obstructive sleep apnea syndrome (OSAS). Furthermore, this study aims at registering objective compliance during MAD therapy.

NCT ID: NCT01525160 Completed - Clinical trials for Obstructive Sleep Apnoea Hypopnoea Syndrome

New Markers to Measure Clotting in Patients With the Obstructive Sleep Apnoea Hypopnoea Syndrome

Start date: October 2011
Phase: N/A
Study type: Observational

Obstructive Sleep Apnoea Hypopnoea Syndrome(OSAHS)affects at least 4% of males and 2% of females. OSAHS is the combination of excessive daytime sleepiness, snoring and apnoeas (stopping breathing at night). As well as affecting tiredness, mood, concentration and quality of life - there is growing concern that it can increase the risk of high blood pressure, heart problems, strokes and thromboses (clots in the veins). It appears that OSAHS may affect the thickness of the blood and cause it to clot more easily it also causes damage to the lining of the blood vessels (endothelial injury). These effects seem independent of other risk factors such as obesity, smoking, family history of clots etc. The investigators are testing new biomarkers: gel point and fractal dimension developed at the Swansea University to measure the 'clotting' of the blood in people with OSAHS and a similar group of people who snore and who are sleepy but do not have OSAHS on sleep studies (Controls) Also markers of vascular inflammation are being measured.

NCT ID: NCT01517750 Completed - Clinical trials for Sleep Apnea, Obstructive

Study to Predict the Need for Humidification Use and Comparison of the Effect of ThermoSmartâ„¢ and no Humidification on Adherence

Start date: January 2012
Phase: N/A
Study type: Interventional

Despite the effectiveness of continuous positive airway pressure (CPAP) in abolishing upper airway obstruction, acceptance of and adherence with therapy has been sub-optimal. One of the only technological advancements shown to increase adherence is heated humidification, now considered part of conventional CPAP therapy in some countries. ThermoSmartâ„¢ is a unique technology developed by Fisher & Paykel Healthcare which utilises a heated breathing tube to deliver optimal humidity in all environments. ThermoSmart has been shown to be superior to conventional humidification in reducing side effects, condensation and titrated pressure as well as increasing total sleep time. However, improved humidity delivery has not lead to significantly increased adherence in unselected obstructive sleep apnea (OSA) patients. A total of 80 patients diagnosed with OSA but naive to CPAP use will be randomized into a single blind, randomized, parallel-arm trial to determine whether the the use of heated humidification will impact therapy adherence.

NCT ID: NCT01508754 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Efficacy of CPAP Treatment on Blood Pressure of Resistant Hypertension Patients With Obstructive Sleep Apnea Syndrome

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The aim is to evaluate the effect of treatment with Continuous Positive Airway Pressure (CPAP) device on clinic and ambulatory blood pressures (BP) of 200 resistant hypertensive patients with moderate-severe obstructive sleep apnea syndrome (OSAS).

NCT ID: NCT01503164 Completed - Clinical trials for Obstructive Sleep Apnea

Effects of Continuous Positive Airway Pressure (CPAP) on Glucose Metabolism

SOMNOS
Start date: September 2011
Phase: N/A
Study type: Interventional

Obstructive sleep apnea affects approximately 2-4% of middle-aged adults in the general population and is associated with several medical conditions including hypertension and coronary artery. Research over the last decade has shown that obstructive sleep apnea may also increase the propensity for insulin resistance, glucose intolerance, and type 2 diabetes mellitus. Positive airway pressure (PAP) is the first line therapy for the treatment of obstructive sleep apnea. While PAP therapy has several favorable effects such as improvements in daytime sleepiness and quality of life, it is not clear whether using PAP therapy can alter metabolic risk. The overall objective of this study is to examine whether treatment of obstructive sleep apnea with positive airway pressure therapy improves glucose tolerance and insulin sensitivity. The primary hypothesis of this study is that PAP therapy of obstructive sleep apnea will improve in insulin sensitivity and glucose metabolism.

NCT ID: NCT01494181 Completed - Clinical trials for Obstructive Sleep Apnea

Unrecognised Obstructive Sleep Apnea Study

OSA
Start date: July 2011
Phase: N/A
Study type: Observational

Plan of investigation: This is an observational cohort study to determine the effect of OSA, independent of other risk factors, on postoperative vascular events. The study is conceived, designed and will be conducted, and analyzed independent to any company. There is no commercial sponsorship.

NCT ID: NCT01482351 Completed - Clinical trials for Obstructive Sleep Apnea

Mild Cognitive Impairment and Obstructive Sleep Apnea

MEMORIES
Start date: September 2012
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) has been linked to increased risk for Alzheimer's disease (AD), but little prospective evidence exists on the effects of OSA treatment in preclinical AD. The objective was to determine if CPAP treatment adherence, controlling for baseline differences, predicts cognitive and everyday function after 1 year in older adults with MCI and to determine effect sizes for a larger trial. The aim of the Mild Cognitive Impairment and Obstructive Sleep Apnea (Memories 1) trial was to determine whether CPAP treatment adherence, controlling for any baseline differences in OSA severity, ApoE4, and other previously identified demographic and patient factors, might predict cognitive and everyday function after 1 year in older adults with amnestic MCI.

NCT ID: NCT01481636 Completed - Clinical trials for Obstructive Sleep Apnea

Assessing the Symptoms of Obstructive Sleep Apnea

OSA
Start date: November 2011
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the correlation between health outcomes associated with the severity of obstructive sleep apnea (OSA) symptomatology, the findings will guide the design of interventional studies.

NCT ID: NCT01476917 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

The ATLAST Long-Term Study

Start date: November 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The Study is a multi-center, prospective, open label, single-arm, three-month, long-term study of the Attune Sleep Apnea System for the treatment of obstructive sleep apnea (OSA). The objective of the study is to monitor long-term use of the Attune Sleep Apnea System.

NCT ID: NCT01471626 Completed - Clinical trials for Obstructive Sleep Apnea

Real-time Attended Home-polysomnography Through Telematic Data Transmission

sleepbox
Start date: December 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to develop an efficient home-based polysomnography device, which allows, through GPRS,continuous real-time monitoring from the sleep lab based in the hospital, in order to decrease the failure rate of home-based recordings.