Safety and Performance Evaluation of CircuLite Synergy

Medtronic Cardiac Rhythm and Heart Failure63 enrolled

Overview

The purpose of the study is to demonstrate the safety and functionality of the CircuLite Synergy Pocket Circulatory Assist Device.

The CircuLite Synergy Pocket Circulatory Assist Device is an implantable miniature, mixed-flow blood pump designed o provide partial left ventricular support in patients with advanced heart failure. Treatment for this patient population currently include lifestyle changes, medicines, transcatheter interventions and surgery, including implantation of mechanical ventricular assist devices (VADs); most of the currently available VADs require highly invasive, high-risk surgical procedures to implant due to large device size, and are therefore generally limited to use in patients with terminal heart failure. The Synergy pump is intended for treatment of patients with New York Heart Association (NYHA) Class III and IV heart failure; it is expected that the pump will provide these patients with 2-3 L/min of additional blood flow, giving adequate cardiac support to increase exercise tolerance and improve patients' quality of life. The pump's small size will allow it to be implanted in a less surgically invasive procedure than used with previous VADs, which should result in a reduction of perioperative morbidity. The device wil be implanted in a left atrial to subclavian artery bypass with the pump being located in the infraclavicular fossa like a pacemaker.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Heart Failure

Interventions

CircuLite Synergy Pocket Circulatory Assist DeviceDEVICE

Goal of successful implantation and follow-up for at least three months

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Maximum tolerable medical therapy including ACE inhibitors and Beta Blockers * NYHA Class III or IV despite maximal tolerable medical therapy * Ambulatory (inpatient or outpatient) * Patients on the heart transplant list (or, not currently listed but otherwise suitable for heart transplant) * Life expectancy of at least 6 months without full VAD support Exclusion Criteria: * Age \>75 years * Exercise tolerance limited by factors other than heart failure * Presence of intra-atrial thrombus * Clinically significant right heart failure * Serum creatinine \>/= 2.5 mg/dl or any dialysis in previous 3 months * Evidence of intrinsic hepatic disease * Previous episode of resuscitated sudden death without subsequent treatment with AICD * Subclavian artery stenosis * Low platelet count, INR that cannot be corrected prior to implant or contraindication to anticoagulation

Locations (11)

UZ Leuven

Leuven, Belgium

German Heart Centre Berlin

Berlin, Germany

Heart Center Cologne University Hospital

Cologne, Germany

University Hospital Freiburg

Outcomes

Primary Outcomes

Safety - Adverse Events

Evaluation of the incidences of device failure or malfunction, adverse events associated with device use, surgical complications with device implant, and demonstration that the device provides adequate circulatory support in advanced HF patients.

Time frame: 3 months

Secondary Outcomes

Change in hemodynamics

Evaluation of changes across time in hemodynamics, exercise tolerance, neurohormones, quality of life, functional capacity and ventricular function to determine the incidence of worsening HF in patients while supported by the CircuLite Synergy Device.

Time frame: 3 months

Data from ClinicalTrials.gov

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