Cardiac Contractility Modulation Therapy in Subjects With Heart Failure With Preserved Ejection Fraction
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 47
- 试验地点
- 17
- 主要终点
- KCCQ change
研究概览
简要总结
This pilot study will evaluate the efficacy and safety of CCM therapy in heart failure patients with baseline EF≥50% (HFpEF) who have New York Heart Association (NYHA) Class II or III symptoms despite appropriate medication.
The terminology of the HF classification HFpEF is based on the 2016 European Society of Cardiology (ESC) Heart Failure Guidelines.
详细描述
This is a pilot clinical study of CCM in addition to optimal medical therapy (OMT) over a 24 week period.The primary endpoint shall be mean change from baseline to 24 weeks in Kansas City Cardiomyopathy Questionnaire (KCCQ) overall score (reflecting integrated information on physical limitations, symptoms, self-efficacy, social interference and quality of life).
This pilot study will collect efficacy and safety data in heart failure patients having NYHA class II and III symptoms despite appropriate medication with baseline ejection fraction equal or greater than 50% (HFpEF populations).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 40 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Inclusion criteria
- •Baseline ejection fraction ≥ 50% (as assessed by echocardiogram within 30 days of enrollment and confirmed by the echo core laboratory).
- •NYHA class II or III symptoms despite receiving stable optimal medical therapy (OMT) for at least 30 days based on patient's medical records (chronic stable, not transient or crescendo heart failure or angina pectoris)
- •Stable optimal medical therapy for Heart failure for 3 months.
- •NT-proBNP > 220 pg/ml for subjects in sinus rhythm or > 600 pg/ml for subjects in atrial fibrillation
- •Has the following (as assessed by the core lab):
- •LAVi ≥ 34 ml/m² or LVH >12mm AND either
- •E/e' ≥ 13 OR
- •septal e' < 7 cm/s or lateral e' <10 cm/s
- •Patient giving informed consent, willing to be available for scheduled study follow-up visits, and able to complete all testing of the study protocol
排除标准
- •Age below 40 or greater than 80
- •Patients with expected lifespan of less than 12 months from time of enrollment
- •Subjects referred to an institution based on a judicial or administrative order
- •Dilated left ventricle, as evidenced by LVEDVI >= 97 mL/m2 (as assessed by the echo core lab)
- •Primary cardiac valvular disease (anything more than grade 2)
- •Congenital or untreated ischemic heart disease
- •Infiltrative / inflammatory / genetic cardiomyopathy as documented in the medical record (e.g. amyloid, hemochromatosis, myocarditis, hypertrophic cardiomyopathy, M. Fabry, cardiac tumor), or persistent large pericardial effusion
- •Unstable or frequent (>1 episode/week) angina pectoris
- •Hospitalization for HF requiring the use of inotropic support or IABP within 30 days of enrollment
- •Systolic Blood Pressure > 160 mmHg
- •Uncorrected severe anemia (e.g. hemoglobin <9g/dL)
- •PR interval greater than 375 ms
- •Exercise tolerance limited due to noncardiac disorders (e.g. deconditioning, severe lung disease, frailty)
- •Scheduled for a cardiac surgery or a PCI procedure, or had a cardiac surgery procedure within 90 days or a PCI procedure within 30 days prior to enrollment
- •Myocardial infarction within 90 days of enrollment
- •Cardioversion within 30 days of enrollment
- •History of significant ectopy either on 12-lead ECG or Holter monitoring (more than 10% PVCs).
- •Heart rate > 110 bpm on ECG for patients with atrial fibrillation
- •Mechanical tricuspid valve
- •Prior heart transplant or ventricular assist device
- •Pregnant or planning to become pregnant during the study
- •Breastfeeding subjects
- •Subject participating in another medical therapy or device related study, unrelated to CCM™, at the same time or within 30 days prior to enrollment into this study
- •Subjects on dialysis, or with documented GFR<30 or with other major medical disorder (e.g. severe anemia, liver failure)
- •Subjects with any active non-cardiac implants
研究组 & 干预措施
CCM therapy
Optimizer SMART
干预措施: Optimizer SMART (Device)
结局指标
主要结局
KCCQ change
时间窗: 24 weeks
Mean change from baseline to 24 weeks in Kansas City Cardiomyopathy Questionnaire (KCCQ) overall score
次要结局
- NT-proBNP(24 weeks)
- NYHA class(24 weeks)
- Echocardiography(24 weeks)