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Apnea clinical trials

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NCT ID: NCT02649933 Terminated - Pregnancy Clinical Trials

Detection of Sleep Apnea Syndrome (OSA) in Pregnant Women and Assessment of Impact of OSA on Pregnancy Course

Start date: November 2015
Phase: N/A
Study type: Observational

To assess prevalence of obstructive sleep apnea during pregnancy and its impact on prgnancy course and materno foetal wellbeing.

NCT ID: NCT02635100 Terminated - Sleep Apnea Clinical Trials

Multinight CPAP for Sleep Apnea Patients

Start date: May 2015
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is a prevalent disorders characterized by intermittent obstructions of the upper airway during sleep. Continuous Positive Airway Pressure (CPAP) has been shown to be the most efficacious treatment for OSA. It consists of a small device that provides positive airway pressure delivered by a mask attached to the patients nose/mouth.

NCT ID: NCT02612038 Terminated - Clinical trials for Obstructive Sleep Apnea

Nasal Expiratory Resistance in Patients With Sleep Apnea and Expiratory Flow Limitation

ExpFLOSA
Start date: May 1, 2016
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is inherently site-specific. In a physiological controlled intervention study, the investigators seek to determine whether applying expiratory resistance can acutely improve ventilation and sleep in patients with expiratory flow limitation (EFL).

NCT ID: NCT02590159 Terminated - Clinical trials for Obstructive Sleep Apnea

Clinical Study for the BONGO NASAL Expiratory Positive Airway Pressure (EPAP) Device in the Treatment of Obstructive Sleep Apnea (OSA)

Start date: November 2015
Phase: N/A
Study type: Interventional

Single center clinical study for the BONGO NASAL EPAP device in the treatment of obstructive sleep apnea for the purpose of obtaining safety and efficacy data

NCT ID: NCT02577445 Terminated - Sleep Apnea Clinical Trials

The remedÄ“® System for the Treatment of Central Sleep Apnea in Daily Practice

TREAT-CSA
Start date: February 2016
Phase: N/A
Study type: Observational

The aim of this post market study is to assess the impact of sleep-disordered breathing on the well-being of patients according to the treatment chosen, i.e. with or without implantation of the remedÄ“® system to treat sleep-disordered breathing.

NCT ID: NCT02573116 Terminated - Clinical trials for Cardiovascular Disease in Obstructive Sleep Apnea

Impact of Treatment of Periodontis on Endothelial Function in Patients With Obstructive Sleep Apnea

EndothSAS
Start date: March 24, 2014
Phase: N/A
Study type: Interventional

Evaluation of the add-on effect on endothelial dysfunction of treatment of periodontitis in patients with chronic periodontitis and severe obstructive sleep apnea treated by CPAP. Patients with and without chronic periodontitis will be treated by CPAP for 20 weeks. At V2 (10 weeks), endothelial dysfunction will be assessed by the Reactive Hyperemia- Peripheral Artery Tone index. The endothelial dysfunction of the patients will be also assessed at V3 (20 weeks) after periodontitis treatment for the group of patients with chronic periodontitis.

NCT ID: NCT02569749 Terminated - Clinical trials for Sleep Apnea/Hypopnea Syndrome

Sleep Apnea Screening

Start date: June 2015
Phase: N/A
Study type: Observational [Patient Registry]

To assess the incidence of Sleep Apnea-Hypopnea Syndrome (SAHS), both obstructive and central, in patients with: 1) pacemaker indication; 2) implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy (CRTD), 3) heart failure and preserved left ventricular ejection fraction (LVEF) and 4) heart failure and reduced LVEF.

NCT ID: NCT02567448 Terminated - Clinical trials for Obstructive Sleep Apnea

Pathophysiology of the Upper Airway in Patients With COPD and Concomitant OSA

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

The purpose of study is to evaluate the physiologic effects of pulmonary tissue/structural changes associated with COPD and upper airway inflammation on upper airway collapsibility. Upper airway collapsibility is closely associated with development of obstructive sleep apnea (OSA), which is a common disease characterized by repetitive collapse of upper airway during sleep, leading to hypoxemia and arousal. OSA has important neurocognitive and cardiovascular consequences, especially in patients with COPD. Participants in this research study will undergo two overnight sleep studies (PSGs), pulmonary function test, and CT scan of the upper airway and chest. The first sleep study will evaluate the sleep breathing disorder and the second sleep study will measure the upper airway collapsibility, called critical closing pressure (Pcrit). Pcrit is measured by a modified continuous positive airway pressure (CPAP) machine which can provide a wide range of pressures between 20 and -20 cmH2O in order to modify upper airway pressure.

NCT ID: NCT02533050 Terminated - Clinical trials for Obstructive Sleep Apnea

Attentional Capacity and Working Memory in Coronary Artery Disease Patients: Impact of the Presence of a Sleep Apnea Syndrome and Chronic Effects of Treatment With CPAP

CAPCORSAS
Start date: August 2014
Phase: N/A
Study type: Interventional

The presence of Obstructive Sleep Apnea Syndrome (OSAS) has a high frequency in patients victims of a coronary artery disease (CAD) (myocardial infarction, revascularization). Unlike patients seen in a sleep Laboratory with an impact on daytime functioning, CAD apneic patients do not complain in their daytime functioning. The objective of this study is to explore whether the objective cognitive assessment measures may be a good marker of the efficacy of CPAP treatment given to non-sleepy apneic CAD patients. Coronary patients with an AHI between 15 and 40 / h will be treated (or not) after randomization with CPAP treatment. The expected results are: CPAP apneic coronary patients should have a positive impact on cognitive performance, particularly on attention span and working memory measured by improvement in the Paced Auditory Serial Addition Test score (PASAT score).

NCT ID: NCT02494102 Terminated - Clinical trials for Obstructive Sleep Apnea

Evaluation of Modafinil vs Placebo for Treatment of Anesthesia Delayed Emergence in Obstructive Sleep Apnea

ModOSA
Start date: February 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether modafinil use in patients with obstructive sleep apnea will improve postoperative delayed emergence after general anesthesia.