Clinical Trials Logo

Sleep Apnea, Obstructive clinical trials

View clinical trials related to Sleep Apnea, Obstructive.

Filter by:

NCT ID: NCT02003729 Recruiting - Clinical trials for Obstructive Sleep Apnea

SIESTA: Home Sleep Study With ApneaDx™ for the Diagnosis of Obstructive Sleep Apnea

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

The SIESTA Home Sleep Study is a pragmatic, multi-centre randomized single-blinded two arm trial, assisted by a Decision Analytic Model, primarily designed to assess the accuracy, effectiveness and cost-effectiveness of diagnosing OSA assisted by ApneaDx™ as compared to PSG as a reference standard.

NCT ID: NCT01936038 Recruiting - Clinical trials for Sleep Apnea, Obstructive

Upper Airway Toning for Improve the Compliance of CPAP

Start date: June 2013
Phase: Phase 1
Study type: Interventional

The obstructive sleep apnoea/hypopnoea syndrome (OSAHS) is a breathing disorder which happens at night and consists of the interruption of airflow for more than five seconds. His current treatment by continuous positive pressure nocturnal machine (CPAP) is not curative and therefore the level of compliance is key to patient improvement. Many patients don´t tolerate CPAP by the numerous side effects involved. The Upper Airway Toning is a compendium of non-invasive techniques that aim to assist tolerance and compliance with the CPAP. These techniques are: oropharyngeal exercises executed actively by the patient for the muscle toning of the upper airways, electrostimulation of the muscles in the floor of the mouth, correction of the tongue position, nasal and bronchial fogging, execution of respiratory gymnastics, therapy myofascial in the oropharyngeal muscles, manual therapy in the cervical column,and massage in the diaphragm. All the techniques together seek for a greater or lesser impact on the upper airways hypotony, the hypotony of the tongue and the soft palate, the jaw retrognathism, the mouth breathing, the vertebrobasilar syndrome, the gastroesophageal reflux, the excessive accumulation of secretions in the upper and lower airways, the obstructive and restrictive respiratory problems, the sleeping posture, the hypertonia of the diaphragm due to the excess effort in trying to overcome the respiratory obstruction. All these disfunctions will make easier for the patient to show side effects in the use of CPAP. There will be a double-blind randomized controlled study with 110 individuals. One group will follow the conventional medical treatment with CPAP and the other group medical treatment plus Upper Airway Toning. After six months, the mean improvement between the two groups will be compared.

NCT ID: NCT01829854 Recruiting - Clinical trials for Obstructive Sleep Apnoea

To Investigate the Incidence of Obstructive Sleep Apnoea in Patient Undergoing Open Heart Surgery

Start date: June 2012
Phase: N/A
Study type: Observational

This is a study to investigate the incidence of Obstructive Sleep Apnoea in Patient undergoing open heart Surgery . This will include enrolment of 400 patient undergoing open heart surgery .

NCT ID: NCT01828216 Recruiting - OSA Clinical Trials

Ambulatory Versus Conventional Approach Diagnosing OSA

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

Very few studies have examined different models of care involving initial ambulatory home-based diagnosis in diagnosing OSA, identifying patients who benefit from CPAP, and reducing the need for PSG. This study aims to assess the role of an ambulatory approach with home diagnostic sleep study. We hypothesize that the ambulatory approach is as good as the conventional approach in managing OSA in terms of improvement of clinical outcome but the former approach will lead to substantial cost savings.

NCT ID: NCT01800786 Recruiting - Clinical trials for Obstructive Sleep Apnea

Memory Consolidation in Obstructive Sleep Apnea

Start date: August 2011
Phase: N/A
Study type: Interventional

The overarching goal of the research proposed here is to test the hypothesis (i) that the pathophysiological mechanisms of OSA lead to deterioration in sleep-dependent memory consolidation across memory systems, with the genetic marker APOε4 as a modulator, and (ii) that CPAP can reverse some or all of these measured memory deficits. In addition, we are exploring which aspects of OSA (e.g., changes in sleep architecture, measures of hypoxemia, or the EEG power spectrum) most likely impact sleep-dependent memory processing.To this end, we are using specific cognitive tasks for which sleep-dependent memory consolidation processes have previously been demonstrated by our group and others. In addition, we are carrying out quantitative EEG power spectral analyses, to delineate abnormal functioning of brain regions with more precision.

NCT ID: NCT01785199 Recruiting - Clinical trials for Obstructive Sleep Apnea

Effects of Head Elevation by a Bed on Sleep-disordered Breathing

Start date: October 2013
Phase: Phase 1
Study type: Interventional

Sleep is known to be a dynamic state of consciousness that is characterized by rapid fluctuations in autonomic activity as well as changes in body postures. Body postures during sleep influence the severity of sleep-disordered breathing because a supine position is associated with an increase in upper airway collapsibility and thus an increase in frequency and duration of snoring and apnea. Use of an adjustable bed to elevate patients' head might improve those conditions. The purpose of the present study is to determine whether use of an automatic adjustable bed is associated with reducing sleep-disordered breathing in patients with suspected obstructive sleep apnea (OSA) due to upper airway problems.

NCT ID: NCT01685736 Recruiting - Hypertension Clinical Trials

Ambulatory Versus Home Blood Pressure Monitoring in Obstructive Sleep Apnea

OSA
Start date: February 2012
Phase: N/A
Study type: Observational

Subjects referred to a sleep clinic had polysomnography (PSG), clinic BP measurements, 24-hour ABP monitoring and HBP monitoring using a device (Microlife WatchBP HomeN) that allows daytime (3 days, 2 duplicate readings/day) and automated nighttime BP measurement (3 nights, 3 readings/night).

NCT ID: NCT01683721 Recruiting - Clinical trials for Obstructive Sleep Apnea

Post-Market Observational Study of the WINX Sleep Therapy for the Treatment of Obstructive Sleep Apnea (OSA)

UNMASK
Start date: September 2012
Phase: N/A
Study type: Observational

The objective of the Study is to observe the use and utility of the Winx Sleep Therapy System in a clinical practice, for the treatment of patients with obstructive sleep apnea (OSA).

NCT ID: NCT01636856 Recruiting - Clinical trials for Primary Snore, Obstructive Sleep Apnea (Mild and Moderate).

Effects of Oropharyngeal Exercises on Patients With Primary Snore, Mild and Moderate Obstructive

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

Randomized study of patients with primary snore, mild and moderate obstructive sleep apnea. Protocol include 40 patients randomized to oropharyngeal exercise or use of nasal dilator, breathing exercise and nasal lavage. The objectives are study the effects of therapy on oropharyngeal in a series of clinical and physiologic and anatomic variables, changes on snore and quality of sleep using Pharyngeal Critical Pressure, Magnetic Resonance, Negative expiratory pressure and snore analyses. Hypothesis that the therapy group (oropharyngeal exercises) will have more modifications compared to the control group.

NCT ID: NCT01634074 Recruiting - Clinical trials for Obstructive Sleep Apnea

Reiterative Development and Evaluation Study of OSA Therapy System

Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate new iterations/generations of the ApniCure sleep therapy device.