Optimized settings for adaptive servo ventilation in patients with severe heart failure based on the echocardiogram
Not Applicable
- Conditions
- heart failure with reduced ejection fraction
- Registration Number
- JPRN-UMIN000044220
- Lead Sponsor
- Tokyo Women's Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Not provided
Exclusion Criteria
The patients who had a respiratory failure, severe pulmonary disease, pure right-sided HF including pulmonary arterial hypertension, neurological or muscular disease, stenotic valvular disease, constrictive pericarditis or pericardial effusion, any intracardiac shunt, and/or intolerance of ASV.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary study end point in the time-to-event analysis was the first event of the composite of death from any cause, or an unplanned hospitalization for worsening chronic heart failure or ventricular tachycardia.
- Secondary Outcome Measures
Name Time Method