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A Study Evaluating an Implantable Cardiac Microcurrent Device in Patients With Chronic Heart Failure

2026年8月27日 更新者:Berlin Heals GmbH

A Double Blind, Randomized, Sham Controlled Parallel-group Study, Evaluating the Performance of the Berlin Heals Cardiac Microcurrent (C-MIC) System With a Subcutaneously Implanted Left Ventricular Lead in Patients With Chronic Heart Failure With Reduced Ejection Fraction Stratified by Disease Etiology

This study evaluates the safety and performance/effectiveness of the C-MIC System, an active implantable medical device designed to treat patients with heart failure with reduced ejection fraction (HFrEF). The system delivers a non-excitatory, constant direct electrical microcurrent (DC) to the heart with the aim of improving cardiac function.

The C-MIC System is intended for use in patients with ischemic or non-ischemic dilated cardiomyopathy who have symptomatic, ambulatory heart failure despite receiving guideline-directed medical therapy. Eligible patients must have a left ventricular ejection fraction (LVEF) between ≥20% and ≤40%.

The device is implanted in the catheterization laboratory using a minimally invasive procedure that does not require open-heart surgery. Following implantation, patients receive C-MIC Therapy for a duration of six months. The therapy is designed to improve left ventricular performance, as well as functional capacity and patient well-being, including 6-minute walk distance, quality of life, and New York Heart Association (NYHA) functional class.

研究概览

研究类型

介入性

注册 (估计的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

INCLUSION CRITERIA

  • Only for Stratum 1: Patients with HFrEF with non-ischemic disease etiology1
  • Only for Stratum 2: Patients with HFrEF with ischemic disease etiology. All Participants

    1. Informed consent in writing obtained from patient.
    2. Ambulatory patients with symptomatic chronic heart failure in NYHA functional class II-IV at the time of screening lasting for more than 1 year based on the date of diagnosis. Participants in NYHA II at screening must have one documented episode of NYHA III during the prior 6 months with either hospitalization or increase of heart failure medication dosage.
    3. Documented worsening heart failure episode within 12 months prior to screening, defined as HF hospitalization, requirement for intravenous diuretic therapy, or escalation of oral diuretic therapy due to clinically significant worsening HF symptoms requiring medical intervention, as evidenced by source documentation.
    4. Patients who have a baseline LVEF of ≥ 20 % and ≤ 40 % in echocardiography as assessed by the core-lab within 30 days prior to device implantation.
    5. Female and male patients aged 18 years to ≤ 80 years.
    6. Patients receiving appropriate, stable guideline-directed medical therapy for heart failure for at least 90 days prior to screening. [Note: Stable therapy is defined as no more than a 50 % increase or 50 % decrease in dose. If a patient is unable to take guideline recommended doses of heart failure medication, documented evidence must be available.]
    7. Patients who are able to perform a 6-minute walk test. At screening, the 6-minute walk test distance is between 100 and 450 m.
    8. Body habitus that, in the opinion of the Investigator, permits safe and feasible implantation of the C-MIC System, including adequate anatomical access and visualization required for the procedure

      EXCLUSION CRITERIA All Participants

  • Patients who are not likely to experience improvement of their chronic heart failure by the microcurrent therapy, because the causes of the disease cannot be influenced even if the patients fulfill the indication for use of the device or if the therapy with the C MIC System is not possible or might be associated with unknown risks:

    1. Patients who have a potentially correctible cause of heart failure, such as severe valvular heart disease or congenital heart disease.
    2. Patients with an indication for a CRT system according to current guidelines.
    3. Patients who have been hospitalized for heart failure which required the use of inotropic support within 90 days before screening.
    4. Patients with systolic blood pressure (SBP) above 150 mmHg and diastolic blood pressure (DBP) above 90 mmHg despite optimal antihypertensive medical treatment.
    5. Patients with SBP < 90 mmHg at screening while not receiving vasopressor therapy, as assessed by the Investigator.
    6. Patients with hemoglobin blood level < 11 g/dL.
    7. Patients with primary severe pulmonary hypertension defined as estimated systolic pulmonary artery pressure (SPAP) > 80 mmHg on screening echocardiography.
    8. Patients who have genetic connective tissue disease (for example Marfan syndrome).
    9. Patients with a prosthetic tricuspid valve.
    10. Patients in whom access for implantation of the leads cannot be obtained (i.e. known venous occlusion, post radiation therapy).
    11. Patients with other anatomical features (e.g., thoracic deformities) that, in the investigator's judgment, would make straightforward device placement unlikely.
    12. Patients with a pacemaker, an ICD system, a CRT system or with a CCM system* [* In case the patient requires a pacemaker or has a CCM device, the impulses given from the device could change the C-MIC System setting into a safe state and stop the microcurrent.]
    13. Current pregnancy or Breast feeding/lactating women
    14. Women of childbearing potential (WOCBP), defined as all women who are physiologically capable of becoming pregnant, unless they are using a highly effective methods of contraception (failure rate < 1 % per year), as determined by the investigator, for at least 2 months prior to C-MIC therapy and continuing until 1 month after completion of therapy
    15. Patients whose exercise tolerance is limited by a condition other than heart failure (e.g. chronic obstructive pulmonary disease, peripheral vascular disease, orthopedic or rheumatologic conditions) or who are unable to participate in a 6 minute walk test.
    16. Patients on immunosuppressive therapy.
    17. Patients with present malignancy.
    18. Patients with an active infection considered by the investigator to be unsafe for the patient's participation in the trial.
    19. Patients with renal dysfunction, i.e., estimated glomerular filtration rate (eGFR) <25 mL/min/1.73 m².
    20. Patients with history or presence of relevant liver diseases or hepatic dysfunction as indicated by abnormal liver function tests at screening and baseline: ALT (SGPT), AST (SGOT), GGT, alkaline phosphatase (ALP) and serum bilirubin > 2 × upper limit of normal (ULN). Increase of these liver enzymes caused by cardiac disorders in the absence of other possible causes of liver damage are not meant by this.
    21. Patients with a history of drug or alcohol abuse within the 12 months prior to screening.
    22. Patients who, in the opinion of the Principal Investigator, are unlikely to comply with the protocol requirements, instructions and trial related restrictions, e.g., uncooperative attitude, inability to return for follow-up visits, psychological illness, and improbability of completing the trial.
    23. Participation in any study of an investigational device or drug within 90 days prior to planned study.
    24. Vulnerable Patients (e.g. patients requiring a legal representative, patients kept in detention, any service within the army, and employees of the sponsor or at an investigator site).
    25. Patients who are not able to avoid the following areas (i.e. due to work): a) Areas with strong magnetic fields. b) Areas with strong external electrical influences. c) Areas with a warning notice "Access prohibited for pacemaker patients" or similar. d) Areas with high temperatures Stratum 2 only (ischemic etiology)
    26. Acute coronary event within 3 months prior to screening (def.: unstable angina or STEMI or NSTEMI).
    27. Evidence of significant myocardial scar or left ventricular aneurysm based on imaging (e.g., echocardiography or other modalities), as assessed by the investigator.
    28. Relevant coronary stenosis with indication for re-vascularization (def.: ≥ 50 % stenosis in LMCA, ≥ 70 % stenosis in LAD, RCA, CX.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
其他:Stratum 1: Ischemic Etiology
Stratum 1a: Active → Inactive Stratum 1b: Inactive → Active
The C-MIC System is implanted subcutaneously using a minimally invasive, non-open-heart procedure performed in a catheterization laboratory. Following randomization, C-MIC Therapy is either inactive or active from Day 1 through Day 180 and active or inactive, respectively, from Day 180 through Day 360.
其他:Stratum 2: Non-Ischemic Etiology
Stratum 2a: Active → Inactive Stratum 2b: Inactive → Active
The C-MIC System is implanted subcutaneously using a minimally invasive, non-open-heart procedure performed in a catheterization laboratory. Following randomization, C-MIC Therapy is either inactive or active from Day 1 through Day 180 and active or inactive, respectively, from Day 180 through Day 360.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change From Baseline in Kansas City Cardiomyopathy Questionnaire Clinical Summary Score at Month 6
大体时间:From baseline to 6 months
The Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (KCCQ-CSS) assesses heart failure symptoms and physical limitations. Scores range from 0 to 100, with higher scores indicating better health status. Change from baseline is calculated as the Month 6 score minus the baseline score; a positive change indicates improvement.
From baseline to 6 months
Change From Baseline in 6-Minute Walk Distance at Month 6
大体时间:From baseline to 6 months
The 6-Minute Walk Test measures functional exercise capacity as the distance, in meters, that a participant can walk in 6 minutes. Change from baseline is calculated as the Month 6 distance minus the baseline distance; a positive change indicates improvement.
From baseline to 6 months
Ordinal Shift From Baseline in New York Heart Association Functional Class at Month 6
大体时间:From baseline to 6 months
New York Heart Association (NYHA) Functional Class is a clinician-assessed, 4-category ordinal classification of heart failure severity: Class I indicates no limitation of physical activity, Class II indicates slight limitation, Class III indicates marked limitation, and Class IV indicates symptoms at rest. A shift to a lower class indicates improvement, and a shift to a higher class indicates worsening.
From baseline to 6 months
Patient Global Assessment of Change Score at Month 6
大体时间:6 months
The Patient Global Assessment of Change is a participant-reported assessment of overall change in health status relative to baseline. It is measured on a 7-point ordinal scale ranging from 1 ("markedly worse") to 7 ("markedly improved"), with 4 indicating "no change." Higher scores indicate a more favorable assessment.
6 months
Percentage of Participants Who Are Echocardiographic Responders at Month 6
大体时间:From baseline to 6 months

An echocardiographic responder is a participant who meets at least 1 of the following criteria at Month 6 compared with baseline:

  • Increase in left ventricular ejection fraction (LVEF) of at least 5 percentage points
  • Improvement in global longitudinal strain (GLS) of at least 2 percentage points, defined as an increase in the absolute magnitude of GLS
  • Relative reduction in left ventricular end-diastolic volume index (LVEDVi) of at least 10%
  • Relative reduction in left ventricular end-systolic volume index (LVESVi) of at least 10% Each participant will be counted once as a responder if at least 1 criterion is met. The outcome will be reported as the percentage of participants classified as echocardiographic responders.
From baseline to 6 months
Change From Baseline in N-Terminal Pro-B-Type Natriuretic Peptide Concentration at Month 6
大体时间:From baseline to 6 months
N-terminal pro-B-type natriuretic peptide (NT-proBNP) is a blood biomarker of heart failure severity and is measured in picograms per milliliter (pg/mL). Change from baseline is calculated as the Month 6 concentration minus the baseline concentration; a negative change indicates a reduction in NT-proBNP.
From baseline to 6 months

次要结果测量

结果测量
措施说明
大体时间
Change in Left Ventricular Ejection Fraction From Month 6 to Month 12
大体时间:From 6 monts to 12 months
Left ventricular ejection fraction (LVEF) is measured by echocardiography and reported as a percentage. Change is calculated as the Month 12 LVEF minus the Month 6 LVEF. A positive value indicates an increase in LVEF, whereas a negative value indicates a decline. This outcome will assess maintenance of the LVEF improvement observed at the end of the initial 6-month treatment period.
From 6 monts to 12 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

有用的网址

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2027年9月1日

研究完成 (估计的)

2028年10月1日

研究注册日期

首次提交

2026年8月10日

首先提交符合 QC 标准的

2026年8月27日

首次发布 (实际的)

2026年8月31日

研究记录更新

最后更新发布 (实际的)

2026年8月31日

上次提交的符合 QC 标准的更新

2026年8月27日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • C-MIC-IV

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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