Central Sleep Apnea Clinical Trial
Official title:
Central Sleep Apnea Treated by CO2 Supplied by a Novel Device
In general, central sleep apnea is not as common as obstructive sleep apnea but it is common in patients with heart failure. It has been repeatedly shown that central sleep apnea worsens the prognosis of heart failure. The current concept in the development of CSA is hypocapnia which causes temporary cessation of respiratory neural output. Different methods for supplement of CO2 have been used to eliminate CSA. However, variation of CO2 concentration during overnight treatment and tight-fitting mask made the treatment uncomfortable. It is important to develop a device with a comfortable mask to supply constant low dose CO2 without breathing difficulty. We recently developed a device for treatment of CSA.
Objective: To determine whether the device could improve sleep quality while eliminating CSA during the overnight study. Methods: Patients with central sleep apnea diagnosed by diaphragm EMG will be recruited in this study. CO2 concentration for treatment would be manually titrated during overnight PSG. Patients were then treated with an effective lowest concentration of CO2 derived from titration under PSG on the third night. The sleep apnea hypopnea index (AHI), central sleep apnea index (CHI), arousal index (ArI), Oxygen desaturation index (ODI), sleep structure, blood pressure, heart rate, diaphragm EMG, treatment side effects and treatment preference were to be observed. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03032029 -
Registry on the Treatment of Central and Complex Sleep-Disordered Breathing With Adaptive Servo-Ventilation
|
||
Completed |
NCT01426776 -
Effect of Heart Valve Replacement on Cheyne-Stokes Respiration
|
N/A | |
Recruiting |
NCT06043830 -
Managing Opioid Related Sleep Apnea With Acetazolamide
|
Phase 2 | |
Completed |
NCT01831128 -
French Cohort Study of Chronic Heart Failure Patients With Central Sleep Apnoea Eligible for Adaptive Servo-Ventilation (PaceWave, AutoSet CS)
|
||
Withdrawn |
NCT02356367 -
French Cohort Study of Chronic Heart Failure Patients With Central Sleep Apnoea Eligible for Adaptive Servo-Ventilation (PaceWave, AutoSet CS, AirCurve 10CS): Predictive Factors of Poor Compliance (FACE)
|
N/A | |
Completed |
NCT01124370 -
Chronic Evaluation of Respicardia Therapy
|
Phase 2 | |
Recruiting |
NCT05949164 -
The IPAd Study: Exploring the Association Between Insomnia and Positive Airway Pressure Adherence in Children
|
||
Completed |
NCT00922168 -
Pre-operative Polysomnography Assessment of Cardiac Surgery Inpatients
|
N/A | |
Completed |
NCT05354401 -
Heated Humidified High Flow Nasal Cannula Oxygen in Obstructive Sleep Apnea in Adolescents
|
N/A | |
Completed |
NCT03425188 -
Post Approval Study of the remedē System
|
||
Recruiting |
NCT03621566 -
Belgian Central Sleep Apnea REgistry
|
||
Completed |
NCT00551499 -
Cardiac Resynchronisation Therapy in Combination With Overdrive Pacing in the Treatment of Central Sleep Apnea in CHF
|
Phase 4 | |
Recruiting |
NCT03884660 -
remedē System Therapy Study
|
||
Terminated |
NCT03085641 -
Treatment of Central Sleep Apnoea in Patients With Heart Failure With Nasal High Flow Therapy (nHFT)
|
N/A | |
Completed |
NCT03226652 -
Heart Function in Patients Assessed for Sleep Apnoea
|
||
Active, not recruiting |
NCT02116140 -
ASV Effects on Myocardial Energetics and Sympathetic Nerve Function in Heart Failure and Sleep Apnea.
|
N/A | |
Completed |
NCT03421704 -
A Prospective Multicenter Registry of Patients With Sleep Disordered Breathing Treated With DreamStation BiPAP autoSV.
|
||
Recruiting |
NCT02919930 -
Interface Selection for Adaptive Servo Ventilation
|
N/A | |
Terminated |
NCT03919344 -
Pathophysiological Study of CSA in Adults With pLVEF
|
N/A | |
Completed |
NCT02034175 -
Comparison of SomnaPatch With Polysomnography in Sleep Disordered Breathing
|
N/A |