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Apnea clinical trials

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NCT ID: NCT01172093 Completed - Diabetes Mellitus Clinical Trials

A Study on the Prevalence of Obstructive Sleep Apnea in Patients With Type II Diabetes Mellitus

Start date: January 2007
Phase: N/A
Study type: Observational

OSA is prevalent among patients with type II DM

NCT ID: NCT01171196 Completed - Clinical trials for Obstructive Sleep Apnea

Questionnaires to Identify Chinese Patients at Risk for Obstructive Sleep Apnea

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

The purpose of this study is to validate the Berlin questionnaire and STOP-BANG (snore, tired, obstruction, pressure, body mass index (BMI), age, neck, gender) as effective screening tools for Chinese subjects who are suspected to have obstructive sleep apnea (OSA).

NCT ID: NCT01164683 Completed - Sleep Apnea Clinical Trials

A Pilot Study of CPAP Adherence Promotion by Peer Buddies With Sleep Apnea

CPAPPs
Start date: July 2010
Phase: N/A
Study type: Interventional

Obstructive sleep apnea (OSA) is a highly prevalent condition in veterans with some estimates as high as 47%. Poor adherence to the primary treatment of OSA -- continuous positive airway pressure (CPAP) therapy - is associated with increased risk for heart attacks, strokes and even death. The investigators plan to improve CPAP adherence in veterans through their interactions with peers who have successfully adopted CPAP therapy. Such "peer-buddies" may promote the well-being of veterans while remaining highly cost-effective when compared to healthcare providers. Our strategy is grounded on the rationale that veterans as a group are ecoculturally more homogenous than expected for the given level of differences in age, gender, ethnicity, or socioeconomic strata. Our long-term objectives are to initiate a larger, multi-site, research study for enhancing CPAP adherence in veterans with OSA. The ultimate goal of this research is to develop a cheap, effective and exportable system of care to promote CPAP adherence in patients with OSA.

NCT ID: NCT01161420 Active, not recruiting - Clinical trials for Obstructive Sleep Apnea

Stimulation Therapy for Apnea Reduction (Www.theSTARtrial.Com)

STAR
Start date: July 2010
Phase: Phase 3
Study type: Interventional

The purpose of this clinical trial is to demonstrate long-term safety and efficacy of the Inspire system. The Inspire Upper Airway Stimulation (UAS) therapy is intended to treat moderate-to-severe obstructive sleep apnea by improving airway patency through stimulation of the hypoglossal nerve. Study objectives include demonstrating that the Inspire system improves key indices of sleep apnea in a pre-specified percentage of patients.

NCT ID: NCT01161381 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome (OSAS)

Evaluation Of Patients With Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS) Based on Nonlinear Analysis Of Respiratory Signals

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

Objective: Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS) is a common sleep disorder requiring the time and money consuming full polysomnography to be diagnosed. Alternative methods for initial evaluation are sought. The investigators aim was the prediction of Apnea-Hypopnea Index (AHI) in patients suspected to suffer from OSAHS using two models based on nonlinear analysis of three biosignals during sleep. Methods: One hundred patients referred to a Sleep Unit underwent full polysomnography. Three nonlinear indices (Largest Lyapunov Exponent, Detrended Fluctuation Analysis and Approximate Entropy) were extracted from three biosignals (airflow from a nasal cannula, thoracic movement and Oxygen saturation) providing input to a data mining application for the creation of predictive models for AHI.

NCT ID: NCT01157286 Unknown status - Clinical trials for OBSTRUCTIVE SLEEP APNEA

Obstructive Apnea in Patients Submitted to Partial Laryngectomy

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

The investigators intend to study the prevalence of obstructive apnea in patients submitted to partial laryngectomy by larynx cancer. Volunteers will be evaluated using polissonografy. We will try to correlate the residual glotic area with the number of apneas per hour.

NCT ID: NCT01156649 Active, not recruiting - Clinical trials for Obstructive Sleep Apnea

Effects of Positive Airway Pressure (PAP) in Children With Obstructive Sleep Apnea (OSA)

OSA
Start date: July 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Obstructive sleep apnea is a problem for a large number of children and can result in problems with thinking patterns, behaviors and sleep if left untreated. Little is known about how positive airway pressure (PAP) therapy might help children who need treatment for obstructive sleep apnea. We will investigate how PAP therapy might be able to improve thinking patterns, behavior and sleep problems in children with obstructive sleep apnea.

NCT ID: NCT01156116 Completed - Diabetes Clinical Trials

Effective Treatment of Sleep Apnea in Prediabetes to Reduce Cardiometabolic Risk

Start date: October 2009
Phase: N/A
Study type: Interventional

Although obstructive sleep apnea (OSA) is associated with impaired glucose tolerance and diabetes, it remains unclear whether OSA treatment with continuous positive airway pressure (CPAP) has metabolic benefits. The objective of this study is to determine the effect of 8-hour nightly CPAP treatment on glucose metabolism in individuals with prediabetes and OSA.

NCT ID: NCT01155271 Active, not recruiting - Obesity Clinical Trials

OBese Patients With Obstructive Sleep Apnea Syndrome(OSAS) and EXercise Training

OBEX1
Start date: July 2010
Phase: N/A
Study type: Interventional

The study was designed to test the following hypotheses: In obese patients with OSAS, the benefit of the combination of exercise training + continuous positive airway pressure (CPAP) will be higher than CPAP alone in term of functional capacity, metabolic, inflammatory, cardiovascular and sleep parameters and quality of life. In obese patients with OSAS, the benefit of training using ventilatory assistance (NIV) during cycloergometer [cycloergometer with NIV] or respiratory muscles training (spirotiger) in addition to cycloergometer [cycloergometer + spirotiger] will be higher than cycloergometer training alone [cycloergometer] in term of functional and exercise capacities. Dyspnea during walking test and respiratory muscle strength at baseline could influence the response to combined exercise training such as [cycloergometer + NIV] or [cycloergometer + spirotiger]

NCT ID: NCT01146782 Completed - Clinical trials for Obstructive Sleep Apnea

Study of a Sleep Apnea System for the Treatment of Obstructive Sleep Apnea

ATLAST
Start date: June 2010
Phase: N/A
Study type: Interventional

This is a prospective study of the Attune Sleep Apnea System for the treatment of obstructive sleep apnea. The objective of the study is to demonstrate safety and effectiveness of the Attune Sleep Apnea System to support FDA marketing clearance of the device.