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Sleep Apnea, Obstructive clinical trials

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NCT ID: NCT01797705 Completed - Clinical trials for Obstructive Sleep Apnea

Revised Algorithm for Next Generation DeVilbiss Healthcare AutoAdjust Continuous Positive Airway Pressure (CPAP)

Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this protocol is to improve the current FDA-approved continuous positive pressure auto-titration algorithm, including treatment precision, residual disease detection characteristics and phenotyping with the DeVilbiss brand AutoAdjust CPAP device.

NCT ID: NCT01797653 Completed - Clinical trials for Obstructive Sleep Apnoea

Randomized-controlled Trial (RCT) on CPAP-withdrawal and Microvascular Function in OSA

Start date: February 2013
Phase: N/A
Study type: Interventional

Randomized controlled trial (therapeutic vs. placebo CPAP) including 46 patients with obstructive sleep apnea (OSA) to define the physiological effects of continuous positive airway pressure (CPAP) therapy withdrawal on myocardial perfusion and dermal and renal microvascular function during a 2 week period.

NCT ID: NCT01796925 Completed - Clinical trials for Sleep Apnea, Obstructive

Targeted Hypoglossal Neurostimulation Study #2

THN2
Start date: February 2013
Phase: N/A
Study type: Interventional

The objective of the study is to confirm the safety and efficacy in patients utilizing the aura6000 System for the treatment of Obstructive Sleep Apnea (OSA).

NCT ID: NCT01796080 Completed - Clinical trials for Patients With Paroxysmal Atrial Fibrillation

The Effect of Simulated Obstructive Apnoea and Hypopnoea on Heart Rhythm in Patients With Paroxysmal Atrial Fibrillation

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

In this randomised controlled cross-over study we will investigate whether intrathoracic pressure changes induced by simulated obstructive apnoea and hypopnoea trigger premature supraventricular and ventricular contractions as well as atrial fibrillation in patients with paroxysmal atrial fibrillation.

NCT ID: NCT01791270 Completed - Clinical trials for Obstructive Sleep Apnea

Obstructive Sleep Apnea (OSA), Hypertension , β1 Subunit of Maxi-k+ Channel and Cardiovascular Risk

OSAS
Start date: February 2010
Phase: N/A
Study type: Observational

To describe the relationship between OSA and clinical Hypertension (performing ABPM), endothelial dysfunction (performing flowmetry), and its relation at the basic research (determining the β1 subunit in Peripheral Leukocytes in peripheral blood). This relation between OSA and HTA has been evaluated in basal conditions and after modifying the pathophysiological role of OSA applying treatment with positive continues pressure (CPAP) during 3 months.

NCT ID: NCT01790477 Completed - Clinical trials for Obstructive Sleep Apnea

Auricular Acupuncture for The Treatment of Post-Tonsillectomy Pain

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

The goal of this study is to assess the role of battlefield acupuncture in the reduction of pain scores status post adult tonsillectomy. Secondary goals of this study include reduction in narcotic usage, decreased nausea and vomiting, and evaluating patient factors that lend an increased risk of worsening pain or improved response with acupuncture.

NCT ID: NCT01786291 Completed - Clinical trials for Obstructive Sleep Apnea

PAP Therapy Sleep Apnea and Exercise

Start date: May 2010
Phase: N/A
Study type: Observational

Positive airway pressure (PAP) therapy is generally offered to patients with obstructive sleep apnea. The investigators suggest that beneficial effects of PAP therapy is by preventing apneas and therefore reducing cardiac and pulmonary morbidities. The investigators sought to verify this by assessing cardiac and pulmonary function during exercise.

NCT ID: NCT01785303 Completed - Clinical trials for Obstructive Sleep Apnea

Multidisciplinary Approach to the Treatment of Insomnia and Comorbid Sleep Apnea

MATRICS
Start date: February 2013
Phase: N/A
Study type: Interventional

The overall goal of this project is to determine the efficacy of a multidisciplinary treatment model for patients with Obstructive Sleep Apnea (OSA) and comorbid Insomnia. Specific Aim 1: To determine the efficacy of a treatment model combining Cognitive Behavioral Therapy (CBT) and Continued Positive Airway Pressure(CPAP) for individuals with OSA and comorbid insomnia. Specific Aim 2: To determine if there are relative benefits in the sequence of treatment initiation. Specific Aim 3: To examine the mechanisms between insomnia symptoms and CPAP adherence.

NCT ID: NCT01780207 Completed - Clinical trials for Obstructive Sleep Apnea

Impact Of Closure Of Patent Foramen Ovale On Apnoea-Hypopnoea-Index, Nocturnal Hypoxemia And Systemic Vascular Function In Patients With Obstructive Sleep Apnoea

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

The purpose of this study in patients with obstructive sleep apnoea (OSA) and concomitant patent foramen ovale (PFO) is to assess the impact of percutaneous PFO closure on nocturnal hypoxemia and apnea/hypopnea, pulmonary and systemic artery pressure, endothelial function and arterial stiffness.

NCT ID: NCT01769807 Completed - Clinical trials for Obstructive Sleep Apnea

Efficacy Study of CPAP on Nitrate and Norepinephrine Levels in Severe and Mild-moderate Sleep Apnea (SABIO)

SABIO
Start date: July 2004
Phase: N/A
Study type: Interventional

Reduced plasma nitrate (NOx) levels and increased urinary norepinephrine (U-NE) levels have been described in severe obstructive sleep apnea (OSA), and are reverted by continuous positive airway pressure (CPAP). The investigators wanted to know the effect of CPAP on these biomarkers in mild-moderate OSA.