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Cheyne-Stokes Respiration clinical trials

View clinical trials related to Cheyne-Stokes Respiration.

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NCT ID: NCT01095679 Completed - Clinical trials for CHEYNE Stokes Respiration

Baclofen and Hypoxia-induced Periodic Ventilation

PERIODIBAC
Start date: March 2010
Phase: Phase 1
Study type: Interventional

Periodic ventilation that includes CHEYNE Stokes ventilation is a pathological pattern characterized by alternating periods of hyperpneas and apnea-hypopneas. It occurs generally during sleep, at high altitude and in hypoxic conditions in healthy subjects, and in some diseases like congestive heart failure. One study conducted on an animal model suggested that baclofen, a drug already used against spasticity in humans, could also be effective against periodic ventilation. The goal of the study is therefore to assess this hypothesis on hypoxia-induced periodic ventilation in healthy subjects during sleep.

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.

NCT ID: NCT00909259 Completed - Sleep Apnea Clinical Trials

Feasibility Study to Determine the Effects of Phrenic Nerve Stimulation in Patients With Periodic Breathing

Start date: October 2007
Phase: Phase 1
Study type: Interventional

The purpose of this feasibility study is to determine the effect of stimulating the phrenic nerve to treat periodic breathing (a pattern of breathing characterized by hyperpneas followed by hypopneas or apneas). Clinically, these physiologic events translate into sleep fragmentation, excessive daytime sleepiness, reduced exercise capacity, and possibly ventricular arrhythmias. Stage 1 of the study is acute in nature, such that subjects will undergo the placement of a stimulation lead, followed by assessment of stimulation of the phrenic nerve using the lead for up to 2 nights of sleep. A sensing lead may also be placed during the initial implant procedure. Observational data will be obtained and stimulation provided using an externalized system connected to the study leads. Following the study, all investigational components will be removed from the patient. Stage 2 of the study is being conducted at one of the participating sites to determine the initial safety of chronic stimulation of the phrenic nerve in a limited number of patients with sleep disordered breathing. It is anticipated that data obtained in this feasibility 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 a multi-center study of chronic phrenic nerve pacing.

NCT ID: NCT00563693 Completed - Heart Failure Clinical Trials

Chronic Heart Failure - Cheyne Stokes Respiration - CS2 (3C-study)

3C
Start date: September 2007
Phase: N/A
Study type: Interventional

An investigation where patients with chronic heart failure and cheyne stokes respiration, treated with adapitve servo ventilator, will improve their cardiac function and quality of life.

NCT ID: NCT00543452 Completed - Cardiac Disease Clinical Trials

Effect of Oxygen on Core Temperature

Start date: February 2005
Phase: N/A
Study type: Interventional

Study of the effect of oxygen on the frequency of central apnea, sleep and body temperature in patients with a cardiac disease

NCT ID: NCT00495196 Completed - Clinical trials for Heart Failure, Congestive

Cardiovascular Responses in Congestive Heart Failure With Cheyne- Stokes Respiration

Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of the trial is to investigate the cardiovascular response to peripheral chemoreceptor stimulation in Congestive Heart Failure with Cheyne- Stokes Respiration

NCT ID: NCT00338078 Completed - Heart Failure Clinical Trials

Nocturnal Oxygen Treatment in Heart Failure and Cheyne-Stokes Respiration

Start date: March 1999
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether oxygen therapy during sleep improves quality of life, exercise capacity and heart function among patients with chronic heart failure and central sleep apnea.