JPRN-UMIN000026510已完成4 期
A Multi-Centre, Randomized Study to Assess the Effects of Adaptive Servo Ventilation (ASV) on Survival and frequency of Cardiovascular (CV) Hospital Admissions in Patients with Heart failure (HF) and Sleep Apnea (SA)- The ADVENT-HF Trial. - The ADVENT-HF Trial
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
研究概览
简要总结
ot released yet
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18years-old 至 100years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Heart failure due to primary valvular heart disease 1.Presence of moderate to severe mitral insufficiency due to intrinsic mitral valve disease 2.Hypertrophic obstructive or restrictive or post partum cardiomyopathy 3.Exercise capacity limited by class IV angina pectoris 4.Acute MI, cardiac surgery, PCI, AICD, or CRT within 3 months of randomization 5.Active myocarditis 6.Planned AICD or CRT 7.Presence of a left-ventricular assist device 8.Transplanted heart or expected to receive a transplanted heart within the next 6 months 9.Pregnancy 10.Current use of ASV or CPAP or treated with any investigational therapy during the last 4 weeks (including approved therapies being used in unapproved indications) 11.A clinical history that would interfere with the objectives of this study or that would in the investigator's opinion preclude safe conclusion of the study 12.Any other medical, social, or geographical factor, which would make it unlikely that the patient will comply with the study procedures (e.g. alcohol abuse, lack of permanent residence, severe depression, disorientation, distant location, or history of non-compliance) 13.Any contraindication to ASV therapy as detailed in the device provider manual
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