NORM-HF Pivotal Study (NORM-HF)
NORM-HF (NORM-guided Congestion Management in Heart Failure) Pivotal Study
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Troy Penz
- 電話番号:+1 617-802-5911
- メール:NORM-HF@fire1foundry.com
研究場所
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California
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Chula Vista、California、アメリカ、91911
- 募集
- Cardiovascular Institute of San Diego
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Sacramento、California、アメリカ、95817
- 募集
- UC Davis
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Florida
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Jacksonville、Florida、アメリカ、32209
- 募集
- University of Florida Health - Jacksonville
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Tampa、Florida、アメリカ、33607
- 募集
- BayCare Health System
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New York
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New York、New York、アメリカ、10032
- まだ募集していません
- Columbia University Irving Medical Center/ New York Presbyterian Hospital
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Ohio
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Cincinnati、Ohio、アメリカ、45219
- 募集
- Christ Hospital Lindner
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Oklahoma
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Tulsa、Oklahoma、アメリカ、74136
- 募集
- Saint Francis Health System
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Pennsylvania
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Philadelphia、Pennsylvania、アメリカ、19104
- 募集
- University of Pennsylvania
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South Dakota
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Sioux Falls、South Dakota、アメリカ、57108
- 募集
- North Central Heart - Avera Hospital
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:防止
- 割り当て:ランダム化
- 介入モデル:階乗代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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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介入なし:Control
control arm - standard medical therapy with guideline directed heart failure management
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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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.
時間枠: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.
時間枠: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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協力者と研究者
出版物と役立つリンク
便利なリンク
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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