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Respiratory Aspiration clinical trials

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NCT ID: NCT01124370 Completed - Sleep Apnea Clinical Trials

Chronic Evaluation of Respicardia Therapy

Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the chronic safety and efficacy of phrenic nerve stimulation on central sleep apnea (CSA). Clinically, CSA events translate into sleep fragmentation, excessive daytime sleepiness, reduced exercise capacity, and possibly ventricular arrhythmias. The study is chronic in nature, such that subjects will undergo the implantation of an implantable pulse generator and stimulation lead. A sensing lead may also be placed during the initial implant procedure. Subjects will be followed for up to six-months on therapy to assess respiratory and heart failure outcomes. Following the six-month therapy visit, subjects will enter into a long-term follow-up phase until the completion of the study. It is anticipated that data obtained in this study will show that the proposed intervention can modify respiration with a low incidence of adverse effects. The results of this trial are intended to be used to develop a subsequent protocol for pivotal study.

NCT ID: NCT01120548 Completed - Heart Failure Clinical Trials

Sleep Apnea Treatment During Cardiac Rehabilitation of Congestive Heart Failure Patients

SATELIT-HF
Start date: September 2010
Phase: N/A
Study type: Interventional

Sleep disordered breathing (SDB) is a frequent comorbidity for heart failure patients. Its prevalence varies according to the seriousness of the condition of the patients, but it is present in approximately 50% of patients. Screening patients for SDB and managing them by providing adapted ventilation therapy should improve their quality of life or even their prognosis. Moreover, SDB lowers nocturnal cardiovascular recovery abilities and leads to an increase in fatigability and, as a result, exercise intolerance in patients with heart failure. Physical training as part of a cardiac rehabilitation programme provides many benefits, including improving patients' exercise capacities. Our hypothesis is that adapted sleep disordered breathing therapy during rehabilitation will lead to an improvement in rehabilitation results.

NCT ID: NCT01111487 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Activity of Inspiratory Muscles With the Use of Positive Pressure in Patients With Chronic Obstructive Pulmonary Disease

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

The objective is to evaluate whether the use of expiratory positive airway pressure (EPAP) reduces the electrical activity of the sternocleidomastoid muscle and enhances the action of the muscle in the patient parasternal ported from Chronic Obstructive Pulmonary Disease. Noting also, if the set pressure level (10 or 15 cmH2O) affects this relationship.

NCT ID: NCT01108575 Completed - Respiratory Failure Clinical Trials

Effect of Inspiratory Muscle Training on Duration of Mechanical Ventilation Support

Start date: May 2010
Phase: Phase 1/Phase 2
Study type: Interventional

A growing body of knowledge has documented that the diaphragm, the primary muscle of breathing, atrophies and weakens within days of instituting mechanical ventilation support. Diaphragm weakness has been implicated as a major contributor to difficulty with weaning, or breathing without ventilator support. This study will test whether instituting a diaphragm strength training rehabilitation program will reduce the time patients require mechanical ventilation in a surgical intensive care setting.

NCT ID: NCT01090804 Unknown status - Lung Disease Clinical Trials

The Effectiveness of BreatheMAX Breathing Device on Secretion Clearance

ESMOSC
Start date: August 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determined effects of BreatheMAX on secretion clearance.

NCT ID: NCT01062854 Completed - Clinical trials for Sleep Disordered Breathing

Effects of Earplugs on Sleep and Sleep Apnea

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

The main goal of this study is to assess whether use of earplugs has any effect on sleep, sleep apnea, and daytime sleepiness in individuals who snore.

NCT ID: NCT01056081 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Inspiratory Muscle Training in Chronic Obstructive Pulmonary Disease

Start date: April 2006
Phase: Phase 3
Study type: Interventional

Uncertainty persists regarding the usefulness of incorporating inspiratory muscle training (IMT) in pulmonary rehabilitation programs for patients with chronic obstructive pulmonary disease. In this study the investigators investigate whether IMT associated with exercise training would be better than exercise training alone, with regard to exercise capacity, inspiratory muscle strength and dyspnea.

NCT ID: NCT01049256 Recruiting - Heart Failure Clinical Trials

The Cyclocapnic Method for Measurement of Chemosensitivity

Start date: January 2008
Phase: Phase 1
Study type: Interventional

We aim to test our method for measuring chemosensitivity (the ventilatory response to a change in carbon dioxide), which uses sinusoidal carbon dioxide stimuli. Hypotheses: - Carbon dioxide sensitivity is dependent on the cycle time over which we administer the gas (frequency). - Chemoreflex gain decreases as deadspace increases.

NCT ID: NCT01044407 Recruiting - Periodic Breathing Clinical Trials

Developing a New, Dynamic, Therapeutic Pacemaker Algorithm for Stabilising Periodic Breathing in Chronic Heart Failure.

Start date: January 2010
Phase: Phase 2
Study type: Interventional

To evaluate whether cardiac output manipulation via a cardiac pacemaker can stabilise ventilation.

NCT ID: NCT01037439 Completed - Clinical trials for Cheyne-Stokes Respiration

Comparison of Modified With Conventional Adaptive Servoventilation Processes

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

The objective of this study is to compare the modified adaptive servoventilation control algorithm of the with the standardised algorithms of routinely-used servoventilation processes (AutoSet CS2) in terms of the effect on obstructive and central events. The aim is to normalise breathing during sleep and hence eliminate the sleep-related breathing disorder, resulting in even more effective treatment of nocturnal breathing disorders in patients with cardiovascular diseases and sleep apnoea, to ensure optimum therapy success.