NORM-HF Pivotal Study (NORM-HF)
NORM-HF (NORM-guided Congestion Management in Heart Failure) Pivotal Study
研究概览
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Troy Penz
- 电话号码:+1 617-802-5911
- 邮箱:NORM-HF@fire1foundry.com
学习地点
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California
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Chula Vista、California、美国、91911
- 招聘中
- Cardiovascular Institute of San Diego
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Sacramento、California、美国、95817
- 招聘中
- UC Davis
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Florida
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Jacksonville、Florida、美国、32209
- 招聘中
- University of Florida Health - Jacksonville
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Tampa、Florida、美国、33607
- 招聘中
- BayCare Health System
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New York
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New York、New York、美国、10032
- 尚未招聘
- Columbia University Irving Medical Center/ New York Presbyterian Hospital
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Ohio
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Cincinnati、Ohio、美国、45219
- 招聘中
- Christ Hospital Lindner
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Oklahoma
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Tulsa、Oklahoma、美国、74136
- 招聘中
- Saint Francis Health System
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Pennsylvania
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Philadelphia、Pennsylvania、美国、19104
- 招聘中
- University of Pennsylvania
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South Dakota
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Sioux Falls、South Dakota、美国、57108
- 招聘中
- North Central Heart - Avera Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
INCLUSION CRITERIA:
- Adults 18 years of age or older.
- 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.
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:
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
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
- NYHA functional class III AND NT-proBNP ≥1000 pg/mL. For patients presenting with atrial fibrillation or flutter, NT-proBNP ≥1,600 pg/mL.
- Patients must be prescribed a daily dose of loop diuretic of 40mg or more furosemide, or equivalent, for the two weeks prior to screening.
- Patients must be able to have their daily dose of loop diuretic be increased by at least 1.5 times.
- IVC diameter within the landing zone of between 14mm and 28mm.
- Minimum IVC landing zone length of 60 mm.
- 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
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.
- Severe right sided valvular disease or a right sided mechanical valve.
- Patients with abdominal circumference of greater than 143 cm (56 inches) at screening.
- Patients with an estimated Glomerular Filtration Rate (eGFR) < 25 mL/min/1.73m2 or receiving ultrafiltration or chronic dialysis.
- 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.
- Significant congenital heart disease that would impair ability to implant the IVC sensor or complicate interpretation of the reading (e.g., fontan circulation physiology).
- 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.
- 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.
- Implanted or planned implantation of a pulmonary artery pressure (PAP) monitor.
- Patients that are pregnant, nursing or planning a pregnancy within 1 year of screening.
- Anticipated life expectancy < 12 months due to another etiology or severity of HF.
- Any condition that, in the opinion of the Investigator, would not allow for implantation or utilization of IVC sensor.
- Current or anticipated participation in any other clinical study during the duration of this study not pre-approved by the Sponsor.
- Patients with active systemic infection at screening.
- 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.
- 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.
- 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.
- Patients who have procedures planned that require venous femoral access within 3 months of the Sensor implantation.
- 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
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 |
|---|---|
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实验性的:Intervention
implant of the sensor, physician directed, patient self-management and guideline directed heart failure management
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Patients will be implanted with an inferior vena cava sensor
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无干预:Control
control arm - standard medical therapy with guideline directed heart failure management
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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 |
|---|---|---|
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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
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Up to 5 years
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The primary safety endpoint is freedom from a composite of clinical endpoints.
大体时间:12 months
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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.
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12 months
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合作者和调查者
出版物和有用的链接
有用的网址
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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