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Obstructive Sleep Apnea (OSA) clinical trials

View clinical trials related to Obstructive Sleep Apnea (OSA).

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NCT ID: NCT00850434 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

Improved Automatic CPAP Algorithm to Treat Obstructive Sleep Apnea (OSA)

Start date: November 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a modified AutoSet algorithm running on research hardware versus the traditional AutoSet algorithm running on an S7 AutoSet Spirit. The study will determine if the modified AutoSet algorithm reacts appropriately to obstructive apnoeas and hypopnoeas and provides suitable levels of positive airway pressure compared to the S7 AutoSet Spirit. The hypothesis is that the modified AutoSet algorithm will be more efficacious than the traditional AutoSet algorithm

NCT ID: NCT00834509 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

Biomarkers for Obstructive Sleep Apnea

BOSA
Start date: April 2008
Phase: N/A
Study type: Observational

The purpose of the study is to: - recruit subjects with untreated sleep apnea; assess overnight changes in their blood and urine chemicals - review the overnight changes in blood and urine chemicals after they have been treated for sleep apnea - assess the overnight changes in blood and urine chemicals in healthy individuals with no sleep problems - compare the amount of fat in the belly using a Magnetic Resonance Imaging (MRI) scanner on all subjects

NCT ID: NCT00773721 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

Foam Mask - Assessment of Bioburden in a New Mask Seal Material

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

Obstructive sleep apnoea (OSA) is characterised by a partial or complete collapse of the upper airway during sleep. The treatment of choice for OSA is Continuous Positive Airway Pressure (CPAP). CPAP acts as a positive airway splint, delivering a fixed positive airway pressure to the upper airway via a tube and mask. Compliance, however, to therapy requires that the mask is suitably comfortable so as not to disturb sleep. A key contributor to comfort is the seal component of the mask system. Current mask seals are mainly silicone elastomers, which though well understood and accepted, are often uncomfortable. It is proposed to replace the solid elastomer with a soft polymer foam. The foam is highly porous, and has open cells at its surface. It is therefore more likely to accumulate biological material with repeated use. The current (silicone) material does not present any problematic bioburden issues. Therefore it is important to investigate whether the foam will present bioburden problems to patients, within specified usage parameters. The aims of this study therefore are: 1. to observe the rate of bacterial accumulation on foam mask seal material (polyether polyurethane,) 2. to determine the replacement interval for a foam mask seal, and 3. assess the comfort and function of a foam mask seal.

NCT ID: NCT00739011 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

Validation of HC250 and HC240 Series.

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

This study is designed to determine the effectiveness of two different CPAP devices. One a standard CPAP which has the ability to store comprehensive compliance and efficacy data and the second a auto adjusting CPAP which uses the energy spectrum analysis of flow signals to automatically adjust CPAP pressure and improve sleep variables.

NCT ID: NCT00706511 Completed - Clinical trials for Obstructive Sleep Apnea (OSA)

Metabolic Study of Sleep Apnea in Men and Women

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

The purpose of this study is to look at the metabolic (use of energy) and hormonal features of sleep problems in men and women.