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NORM-HF Pivotal Study (NORM-HF)

NORM-HF (NORM-guided Congestion Management in Heart Failure) Pivotal Study

This is an international, multi-center, prospective, randomized, open-label blinded endpoint study designed to demonstrate that use of the FIRE1 NORM™ System in the management of New York Heart Association Class II/III HF patients is superior for reducing the combined endpoint of worsening HF events and cardiovascular mortality compared to standard of care treatment. Patients will be randomized in a 1:1 ratio to receive either NORM™ System and guided heart failure management (intervention group) or usual standard of care with guided heart failure management (control group).

研究概览

研究类型

介入性

注册 (估计的)

800

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

学习地点

    • California
      • Chula Vista、California、美国、91911
        • 招聘中
        • Cardiovascular Institute of San Diego
      • Sacramento、California、美国、95817
        • 招聘中
        • UC Davis
    • Florida
      • Jacksonville、Florida、美国、32209
        • 招聘中
        • University of Florida Health - Jacksonville
      • Tampa、Florida、美国、33607
        • 招聘中
        • BayCare Health System
    • New York
      • New York、New York、美国、10032
        • 尚未招聘
        • Columbia University Irving Medical Center/ New York Presbyterian Hospital
    • Ohio
      • Cincinnati、Ohio、美国、45219
        • 招聘中
        • Christ Hospital Lindner
    • Oklahoma
      • Tulsa、Oklahoma、美国、74136
        • 招聘中
        • Saint Francis Health System
    • Pennsylvania
      • Philadelphia、Pennsylvania、美国、19104
        • 招聘中
        • University of Pennsylvania
    • South Dakota
      • Sioux Falls、South Dakota、美国、57108
        • 招聘中
        • North Central Heart - Avera Hospital

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:

  1. Adults 18 years of age or older.
  2. Provide informed consent for participation in the clinical study and be willing and able to comply with the required assessments, treatment instructions, and clinical follow-up visits according to the specified schedule.
  3. Patients meeting diagnostic criteria for HF diagnosis for greater than 90 days and are on optimally tolerated medical therapy for at least 30 days, as recommended according to current AHA/ACC/HFSA or ESC HF guidelines with any intolerance or contraindications documented, regardless of ejection fraction, as evidenced by meeting either 3a, 3b OR 3c criterion below:

    1. NYHA functional class II with documented HF decompensation within the previous 12 months resulting in a primary HF hospitalization, HF treatment in a hospital day-care setting or unscheduled visit to a healthcare provider for administration of an intravenous diuretic to treat HF AND NT-proBNP ≥1000 pg/mL. For those patients presenting with atrial fibrillation or flutter, NT-proBNP ≥1,600 pg/mL.

      OR

    2. NYHA functional class III with documented HF decompensation within the previous 12 months resulting in a primary HF hospitalization, HF treatment in a hospital day-care setting or unscheduled visit to a healthcare provider for administration of an intravenous diuretic to treat HF AND NT-proBNP ≥ 600 pg/mL. For patients presenting with atrial fibrillation or flutter, NT-pro BNP ≥900 pg/mL.

      OR

    3. NYHA functional class III AND NT-proBNP ≥1000 pg/mL. For patients presenting with atrial fibrillation or flutter, NT-proBNP ≥1,600 pg/mL.
  4. Patients must be prescribed a daily dose of loop diuretic of 40mg or more furosemide, or equivalent, for the two weeks prior to screening.
  5. Patients must be able to have their daily dose of loop diuretic be increased by at least 1.5 times.
  6. IVC diameter within the landing zone of between 14mm and 28mm.
  7. Minimum IVC landing zone length of 60 mm.
  8. Patients have sufficient cellular and/or Wi-Fi Internet coverage at home and can access the internet on a phone or a computer at home.

EXCLUSION CRITERIA

  1. Presence of advanced end stage HF, suggested by but not limited to:

    • Persistent NYHA functional class IV HF (ACC/AHA/ESC).
    • Current treatment with intravenous vasopressors or inotropes.
    • Received, or are likely to receive in the next 6 months, an advanced therapy (e.g., mechanical circulatory support or cardiac transplant or previously listed for transplant).
    • Receiving end of life HF care.
  2. Severe right sided valvular disease or a right sided mechanical valve.
  3. Patients with abdominal circumference of greater than 143 cm (56 inches) at screening.
  4. Patients with an estimated Glomerular Filtration Rate (eGFR) < 25 mL/min/1.73m2 or receiving ultrafiltration or chronic dialysis.
  5. Presence of end stage hypertrophic cardiomyopathy, end stage restrictive cardiomyopathy, end stage pericardial constriction, end stage cardiac amyloidosis, or other infiltrative cardiomyopathy such as hemochromatosis or sarcoidosis.
  6. Significant congenital heart disease that would impair ability to implant the IVC sensor or complicate interpretation of the reading (e.g., fontan circulation physiology).
  7. Major non-heart-failure-related CV event (i.e., unstable angina, Type 1 myocardial infarction (MI), percutaneous coronary intervention, open heart surgery, or stroke, etc.) within 90 days prior to consent.
  8. Implanted with Cardiac Resynchronization Therapy (CRT)-Pacemaker (CRT-P), CRT Defibrillator (CRT-D), Cardiac Contractility Modulation (CCM), or implantable neuromodulation devices used to treat HF symptoms within 90 days prior to consent.
  9. Implanted or planned implantation of a pulmonary artery pressure (PAP) monitor.
  10. Patients that are pregnant, nursing or planning a pregnancy within 1 year of screening.
  11. Anticipated life expectancy < 12 months due to another etiology or severity of HF.
  12. Any condition that, in the opinion of the Investigator, would not allow for implantation or utilization of IVC sensor.
  13. Current or anticipated participation in any other clinical study during the duration of this study not pre-approved by the Sponsor.
  14. Patients with active systemic infection at screening.
  15. Patients with hypersensitivity or allergy to antiplatelet agents or Sensor components (Nitinol, Polyurethane [PU], Nylon, Polyethylene Terephthalate [PET], and Gold) or contrast media that will not be managed with a clinical site-specific allergy protocol.
  16. Unable to tolerate dual antiplatelet therapy for at least 30 days following implant of the respective sensor or unable to continue oral anticoagulation if currently prescribed.
  17. Patients with an in vivo IVC filter, abnormal IVC or femoral venous anatomy, known congenital malformation or absence of IVC, or occlusive or free-floating thrombus in the IVC, iliac, or common femoral veins.
  18. Patients who have procedures planned that require venous femoral access within 3 months of the Sensor implantation.
  19. Patients with pulmonary embolism, venous thrombosis, or thromboembolism in the 6 months prior to screening and/or with ongoing concerns of hypercoagulability due to underlying conditions e.g., thrombophilia.

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:预防
  • 分配:随机化
  • 介入模型:阶乘赋值
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention
implant of the sensor, physician directed, patient self-management and guideline directed heart failure management
Patients will be implanted with an inferior vena cava sensor
无干预:Control
control arm - standard medical therapy with guideline directed heart failure management

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
The primary efficacy endpoint is a composite total number of CV death and worsening HF events, as adjudicated by an independent CEC.
大体时间:Up to 5 years
Up to 5 years
The primary safety endpoint is freedom from a composite of clinical endpoints.
大体时间:12 months
Including freedom from procedure-related and sensor-related SAEs and serious complications including clinically significant perforation of the IVC, symptomatic caval thrombosis, or device embolization after the device implantation as adjudicated by an independent CEC and core imaging laboratory.
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 (实际的)

2026年5月29日

初级完成 (估计的)

2029年8月1日

研究完成 (估计的)

2033年12月1日

研究注册日期

首次提交

2026年4月28日

首先提交符合 QC 标准的

2026年5月4日

首次发布 (实际的)

2026年5月8日

研究记录更新

最后更新发布 (实际的)

2026年8月25日

上次提交的符合 QC 标准的更新

2026年8月21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

  • TF05-CID01

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

是的

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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