Introducing the Revivent System

  • Remodel Heart Failure
  • Regain Function
  • Renew Life

Revivent Therapy – Addressing a Treatment Gap for Advanced Heart Failure

Patients who experience an LAD (Left Anterior Descending artery) STEMI, or ST-elevation myocardial infarction, suffer a severe type of heart attack caused by complete blockage of a major coronary artery. This blockage drastically reduces blood flow to the heart muscle, leading to extensive tissue damage if not treated promptly.

Such events often result in structural distortion and remodeling of the left ventricle, ultimately progressing to advanced heart failure with reduced ejection fraction.

The Revivent System is designed to treat patients with ischemic heart failure and reduced ejection fraction resulting from extensive left ventricular scarring. These patients typically have a dilated left ventricle and have shown a suboptimal response to guideline-directed medical therapy. The goal of the Revivent procedure is to restore the shape and reduce the volume of the left ventricle, thereby improving overall cardiac function and performance.

Approximately 140k us prevalent STEMI patients are appropriate for Revivent due to anterior scarring, reduced ejection fraction, and limited capacity for physical activity.

  • Remodel

    …the left ventricle to restore the shape, size, and volume of the heart.

  • Regain

    …cardiac performance by removing scarred tissue less invasively.

  • Renew

    …Quality of Life (QoL) for heart failure patients.​

Heart failure Treatment options

RELIVE Clinical Trial

Randomized Evaluation of Less Invasive Ventricular Enhancement or the RELIVE clinical study has been initiated in the United States to assess the safety and efficacy of the BioVentrix Revivent System plus Guideline Directed Medical Therapy (GDMT) compared to GDMT alone for the treatment of LV anterior/apical scar/aneurysm with possible additional involvement of the lateral, septal, and/or inferior regions in patients with symptomatic heart failure.

  • Prospective, multi-center, dual-arm pivotal study
  • 2:1 allocation ratio
  • 135 patients
    • 90 will be treated with BioVentrix Revivent System
    • 45 will be included in an active control group.