DRKS00013707
Completed
未知
Short term effects of adaptive servoventilation and continuous positive airway pressure in patients with central sleep apnea and Cheyne-Stokes Respiration
Klinik für Schlafmedizin und neuromuskuläre Erkrankungen Universitätsklinikum Münster0 sites40 target enrollmentMarch 16, 2018
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- I50.1
- Sponsor
- Klinik für Schlafmedizin und neuromuskuläre Erkrankungen Universitätsklinikum Münster
- Enrollment
- 40
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a. Age \> 18 years (no age limit) (Group 1, 2 and 3\)
- •b. able to consent (Group 1, 2 and 3\)
- •c. predominant central sleep apnoea as defined as AHI\>15/h and \>50% central events and a central AHI \>10/h derived from full overnight attended polysomnography (Group 1, 2 and 3\)
- •d. Diagnosis of Nizza class I pumonary arterial Hypertension \-PAH\- and heart failure with reduced ejection fraction \-HFrEF\- according to the most recent Guidelines of the European Society of Cardiology (ESC); \>12 weeks since the diagnosis of HFrEF / PAH has been made; no hospitalisation for HF in the last 4 weeks; optimal medical therapy in accordance with the most recent Guidelines of the European Society of Cardiology (ESC) with no change in medication in the last 4 weeks and combination therapy for both PAH and HFrEF \-where there was no treatment with combination therapy in PAH patients or with beta blockers or ACE Inhibitors/ARBs in HFrEF, then the reason must be documented\-) (Group 1 and 2\)
- •e. Controls (matched for age and gender) with idopathic central sleep apnoea with normal findings on echocardiogram, electrocardiogram and normal levels of natriuretic peptide hormone (Group 3\)
Exclusion Criteria
- •\- other severe internistic pre\-existing conditions, especially insulin\-dependent diabetes or severe renal impairment \-intake of opiods
- •\- severe psychiatric pre\-existing conditions
Outcomes
Primary Outcomes
Not specified
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