Cheyne-Stokes Respiration Clinical Trial
Official title:
Comparison of a Modified Adaptive Servoventilation With Conventional Adaptive Servoventilation Processes in Terms of Efficacy Against Complex Nocturnal Breathing Disorders
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.
Patients with cardiovascular disorders frequently suffer from sleep-related respiratory disorders (SRRD), such as obstructive sleep apnea (OSA) or a specific form of central sleep apnea, Cheyne-Stokes breathing (CSB, periodic breathing). However there is also a significant incidence of complex nocturnal breathing disorders, with both obstructive and central components. Sleep-related breathing disorders of this kind cause decreases in arterial oxygen saturation through brief hypopneas and apneas. Disturbed breathing also causes the patient to wake frequently during the night (arousals), usually during the hyperventilatory phase of CSB. Repeated arousals cause fragmentation of sleep, and therefore a deep sleep deficit. This leads to increased sleepiness during the day and impaired cognitive performance. Previous studies have shown that Cheyne-Stokes breathing can be treated effectively with adaptive servoventilation. An enhancement to the routinely used algorithm (AutoSet CS2) has been created which allows the algorithm to differentiate between obstructive events and Cheyne-Stokes breathing, and better respond to apneas and hypopneas to eliminate the sleep-related breathing disorder and normalise breathing during sleep. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01426776 -
Effect of Heart Valve Replacement on Cheyne-Stokes Respiration
|
N/A | |
| Completed |
NCT01175031 -
Comparison of Breathing Event Detection by a Continuous Positive Airway Pressure Device to Clinical Polysomnography
|
N/A | |
| Completed |
NCT01199042 -
Bipap autoSV Advanced in Central Apnea Patients
|
N/A | |
| Completed |
NCT00909259 -
Feasibility Study to Determine the Effects of Phrenic Nerve Stimulation in Patients With Periodic Breathing
|
Phase 1 | |
| Completed |
NCT01465971 -
Monitoring of the Cerebral Tissue Oxygenation and Perfusion in the Adapting Climber During Sleep in High Altitude
|
N/A | |
| Terminated |
NCT00694720 -
Evaluation of the Effect of AVE0657 in Cheynes-Stokes Breathing Syndrome Patients
|
Phase 2 | |
| Completed |
NCT00495196 -
Cardiovascular Responses in Congestive Heart Failure With Cheyne- Stokes Respiration
|
N/A | |
| Terminated |
NCT03085641 -
Treatment of Central Sleep Apnoea in Patients With Heart Failure With Nasal High Flow Therapy (nHFT)
|
N/A | |
| Completed |
NCT03421704 -
A Prospective Multicenter Registry of Patients With Sleep Disordered Breathing Treated With DreamStation BiPAP autoSV.
|
||
| Completed |
NCT00543452 -
Effect of Oxygen on Core Temperature
|
N/A | |
| Completed |
NCT02034175 -
Comparison of SomnaPatch With Polysomnography in Sleep Disordered Breathing
|
N/A | |
| Recruiting |
NCT01212705 -
Effect of Adaptive Servoventilation on Cardiac Function in Chronic Heart Failure and Cheyne-Stokes Respiration
|
N/A |