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NORM-HF Pivotal Study (NORM-HF)

21 de agosto de 2026 actualizado por: Foundry Innovation & Research 1, Limited (FIRE1)

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).

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

800

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • California
      • Chula Vista, California, Estados Unidos, 91911
        • Reclutamiento
        • Cardiovascular Institute of San Diego
      • Sacramento, California, Estados Unidos, 95817
        • Reclutamiento
        • UC Davis
    • Florida
      • Jacksonville, Florida, Estados Unidos, 32209
        • Reclutamiento
        • University of Florida Health - Jacksonville
      • Tampa, Florida, Estados Unidos, 33607
        • Reclutamiento
        • BayCare Health System
    • New York
      • New York, New York, Estados Unidos, 10032
        • Aún no reclutando
        • Columbia University Irving Medical Center/ New York Presbyterian Hospital
    • Ohio
      • Cincinnati, Ohio, Estados Unidos, 45219
        • Reclutamiento
        • Christ Hospital Lindner
    • Oklahoma
      • Tulsa, Oklahoma, Estados Unidos, 74136
        • Reclutamiento
        • Saint Francis Health System
    • Pennsylvania
      • Philadelphia, Pennsylvania, Estados Unidos, 19104
        • Reclutamiento
        • University of Pennsylvania
    • South Dakota
      • Sioux Falls, South Dakota, Estados Unidos, 57108
        • Reclutamiento
        • North Central Heart - Avera Hospital

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación factorial
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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
Sin intervención: Control
control arm - standard medical therapy with guideline directed heart failure management

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The primary efficacy endpoint is a composite total number of CV death and worsening HF events, as adjudicated by an independent CEC.
Periodo de tiempo: Up to 5 years
Up to 5 years
The primary safety endpoint is freedom from a composite of clinical endpoints.
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Enlaces Útiles

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

29 de mayo de 2026

Finalización primaria (Estimado)

1 de agosto de 2029

Finalización del estudio (Estimado)

1 de diciembre de 2033

Fechas de registro del estudio

Enviado por primera vez

28 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 de mayo de 2026

Publicado por primera vez (Actual)

8 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

25 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

21 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • TF05-CID01

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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