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Clinical Trial to Evaluate the the ReliantHeart HeartAssist 5® VAD System in Patients Awaiting Heart Transplantation

Primary Purpose

Heart Failure, Cardiac Failure, Congestive Heart Failure

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
HeartAssist 5® VAD System
Control VAD
Sponsored by
ReliantHeart Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring heart assist device, ventricular assist device

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Able to sign Informed Consent.
  2. Age ≥ 18
  3. Body Surface Area (BSA) ≥ 1.2 m2.
  4. Cardiac transplant candidate, defined as: Listed for cardiac transplant, and designated by the institution's multidisciplinary transplant committee as appropriate forLVAD Bridge-to-Transplantation therapy, or Designated by the institutions's multidisciplinary transplant committee as: 1) an appropriate candidate for LVAD Bridge-to transplant therapy, and 2) An inappropriate candidate for LVAD destination therapy
  5. LVAD implantation has been approved by the institution's multidisciplinary transplant committee.
  6. Patient is NYHA Class IV.
  7. Able to return to the clinical site for all routine follow up visits.

Exclusion Criteria:

  1. Cardiothoracic surgery within 30 days prior to enrollment.
  2. Acute Myocardial Infarction within 14 days prior to enrollment.
  3. Prior cardiac transplantation, left ventricular reduction surgery, cardiomyoplasty or left ventricular assist device.
  4. Mechanical, animal, or human tissue heart valve.
  5. History of untreated abdominal or thoracic aortic aneurysm > 5 cm.
  6. On ventilator support for > 72 hours within four days immediately prior to enrollment.
  7. Ongoing mechanical circulatory support other than an intra-aortic balloon pump (IABP).
  8. Proven history of pulmonary embolism within 90 days of enrollment.
  9. Moderate to severe aortic insufficiency as determined by echocardiogram without plans for correction during pump implantation surgery.
  10. Requires aortic, mitral, tricuspid or pulmonary valve replacements (including Bioprosthetic valves) or left ventricular (LV) aneurysm resection.
  11. Uncorrected thrombocytopenia or generalized coagulopathy (e.g., platelets <100,000, INR > 1.6 or PTT > 2.5 times control in the absence of anticoagulation therapy)
  12. Severe right ventricular failure as defined by the anticipated need for right ventricular assist device (RVAD) support OR extracorporeal membrane oxygenation (ECMO) at the time of implantation OR right atrial pressure > 20 mmHg while on multiple inotropes.
  13. Significant renal dysfunction defined as > 3.5 mg/dl or requires hemo or peritoneal dialysis for renal failure (excluding ultra-filtration for fluid removal).
  14. Evidence of intrinsic hepatic disease defined as liver enzyme values (AST, ALT and LDH that are > 3 times the upper limit of normal) OR a total bilirubin > 3 mg/dl OR biopsy proven liver cirrhosis or portal hypertension.
  15. Pregnancy
  16. Active systemic infection prior to study enrollment not yet resolved by treatment. Active Systemic Infection is defined by any one of the following in spite of antibiotic, antiviral or antifungal treatment: 2 or more consecutive positive cultures; elevated temperature > 37.2 (°C) and white blood cell count > 11.0 (103/ml); hypotension, tachycardia and generalized malaise.
  17. Stroke within 90 days prior to enrollment OR patient has a history of cerebral vascular disease with > 80% extra cranial stenosis documented by carotid Doppler study during transplant evaluation
  18. Modified Rankin Scale score of ≥ 2 or has any neurologic disability as confirmed by imaging (CT or MRI).
  19. Significant lower extremity peripheral vascular disease accompanied by rest pain or leg ulceration.
  20. Intolerant to anticoagulant or antiplatelet therapies or any other peri- or postoperative therapy that the investigator may administer based upon the patient's health status.
  21. Psychiatric disorder, or other psychosocial behavior that is likely to impair compliance with the study protocol.
  22. Receiving therapy with an investigational intervention or participating in any other clinical investigation at the time of enrollment.
  23. Condition, other than heart failure, that may limit survival to less than three (3) years and/or would exclude cardiac transplantation.
  24. Unwilling or unable to comply with any study requirement.

Sites / Locations

  • University of California San Francisco
  • University of Stanford
  • University of Miami
  • University of Chicago Medical Center
  • Indiana University Health, Inc. d/b/a Methodist Research Institute
  • St. Vincent Hospital & Health Care Center
  • Jewish Hospital
  • Minneapolis Heart Institute Foundation
  • Mayo Clinic Hospital - Saint Mary's Campus
  • University of Pennsylvania
  • CHI St. Luke's Baylor College of Medicine Medical Center
  • Houston Methodist Hospital
  • University of Texas Health Science Center
  • Providence Sacred Heart Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

HeartAssist 5® VAD System

Control VAD

Arm Description

Implant of the HeartAssist 5® VAD System

Outcomes

Primary Outcome Measures

The primary endpoint is success at 180 days
Success at 180 days is defined as alive on the original device, transplanted or explanted for heart recovery and alive 60 days after device explant.

Secondary Outcome Measures

Adverse Events
Device safety will be reported as the frequency of each adverse event, (including device failure, device malfunction or unanticipated adverse device effects) and the rate of adverse events per patient year.
Quality of Life
Quality of life data, as measured by the EuroQol (EQ-5D) will be summarized and analyzed, for both groups, comparing data at baseline and study intervals.
Functional Status
NYHA and six-minute walk analysis will be reported by group for data at pre-implant and at study-defined intervals.
Neurologic Status
Evaluation of any change in Modified Rankin Scale from baseline to 180-days post-implant or device explant.

Full Information

First Posted
July 24, 2014
Last Updated
July 16, 2018
Sponsor
ReliantHeart Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02205411
Brief Title
Clinical Trial to Evaluate the the ReliantHeart HeartAssist 5® VAD System in Patients Awaiting Heart Transplantation
Official Title
A Prospective, Randomized, Multicenter Clinical Trial to Evaluate the Safety and Efficacy of the HeartAssist 5® VAD System Compared to the Thoratec HeartMate II® VAD and HeartWare® HVAD for Left Ventricular Support in Patients Awaiting Cardiac Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Terminated
Why Stopped
Inability to timely enroll.
Study Start Date
September 2014 (undefined)
Primary Completion Date
March 2018 (Actual)
Study Completion Date
March 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ReliantHeart Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to evaluate the safety and effectiveness of the ReliantHeart HeartAssist 5® VAD System in patients listed for heart transplantation and at risk of death from refractory end-stage heart failure.
Detailed Description
The HeartAssist 5® VAD System is intended for use as a bridge to heart transplantation and will be compared to the HeartMate II and HVAD devices. Patients that meet the study criteria will be randomized 1:1 to either the HeartAssist 5® VAD System (treatment group) or control group (HeartMate II and HVAD). The physician will have the option to choose which control device to implant. The primary objective of the study is to show non-inferiority of the HeartAssist 5® (treatment group) to the control group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Cardiac Failure, Congestive Heart Failure, Heart Failure, Left-sided
Keywords
heart assist device, ventricular assist device

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HeartAssist 5® VAD System
Arm Type
Experimental
Arm Description
Implant of the HeartAssist 5® VAD System
Arm Title
Control VAD
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
HeartAssist 5® VAD System
Intervention Description
The HeartAssist 5® VAD System is a small, implantable pump that is designed to increase blood flow for patients who have heart failure. The device is intended to support patients in the hospital or at home.
Intervention Type
Device
Intervention Name(s)
Control VAD
Intervention Description
The HeartMate II® VAD or HVAD®
Primary Outcome Measure Information:
Title
The primary endpoint is success at 180 days
Description
Success at 180 days is defined as alive on the original device, transplanted or explanted for heart recovery and alive 60 days after device explant.
Time Frame
180 days
Secondary Outcome Measure Information:
Title
Adverse Events
Description
Device safety will be reported as the frequency of each adverse event, (including device failure, device malfunction or unanticipated adverse device effects) and the rate of adverse events per patient year.
Time Frame
180 days
Title
Quality of Life
Description
Quality of life data, as measured by the EuroQol (EQ-5D) will be summarized and analyzed, for both groups, comparing data at baseline and study intervals.
Time Frame
180 days
Title
Functional Status
Description
NYHA and six-minute walk analysis will be reported by group for data at pre-implant and at study-defined intervals.
Time Frame
180 days
Title
Neurologic Status
Description
Evaluation of any change in Modified Rankin Scale from baseline to 180-days post-implant or device explant.
Time Frame
180 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Able to sign Informed Consent. Age ≥ 18 Body Surface Area (BSA) ≥ 1.2 m2. Cardiac transplant candidate, defined as: Listed for cardiac transplant, and designated by the institution's multidisciplinary transplant committee as appropriate forLVAD Bridge-to-Transplantation therapy, or Designated by the institutions's multidisciplinary transplant committee as: 1) an appropriate candidate for LVAD Bridge-to transplant therapy, and 2) An inappropriate candidate for LVAD destination therapy LVAD implantation has been approved by the institution's multidisciplinary transplant committee. Patient is NYHA Class IV. Able to return to the clinical site for all routine follow up visits. Exclusion Criteria: Cardiothoracic surgery within 30 days prior to enrollment. Acute Myocardial Infarction within 14 days prior to enrollment. Prior cardiac transplantation, left ventricular reduction surgery, cardiomyoplasty or left ventricular assist device. Mechanical, animal, or human tissue heart valve. History of untreated abdominal or thoracic aortic aneurysm > 5 cm. On ventilator support for > 72 hours within four days immediately prior to enrollment. Ongoing mechanical circulatory support other than an intra-aortic balloon pump (IABP). Proven history of pulmonary embolism within 90 days of enrollment. Moderate to severe aortic insufficiency as determined by echocardiogram without plans for correction during pump implantation surgery. Requires aortic, mitral, tricuspid or pulmonary valve replacements (including Bioprosthetic valves) or left ventricular (LV) aneurysm resection. Uncorrected thrombocytopenia or generalized coagulopathy (e.g., platelets <100,000, INR > 1.6 or PTT > 2.5 times control in the absence of anticoagulation therapy) Severe right ventricular failure as defined by the anticipated need for right ventricular assist device (RVAD) support OR extracorporeal membrane oxygenation (ECMO) at the time of implantation OR right atrial pressure > 20 mmHg while on multiple inotropes. Significant renal dysfunction defined as > 3.5 mg/dl or requires hemo or peritoneal dialysis for renal failure (excluding ultra-filtration for fluid removal). Evidence of intrinsic hepatic disease defined as liver enzyme values (AST, ALT and LDH that are > 3 times the upper limit of normal) OR a total bilirubin > 3 mg/dl OR biopsy proven liver cirrhosis or portal hypertension. Pregnancy Active systemic infection prior to study enrollment not yet resolved by treatment. Active Systemic Infection is defined by any one of the following in spite of antibiotic, antiviral or antifungal treatment: 2 or more consecutive positive cultures; elevated temperature > 37.2 (°C) and white blood cell count > 11.0 (103/ml); hypotension, tachycardia and generalized malaise. Stroke within 90 days prior to enrollment OR patient has a history of cerebral vascular disease with > 80% extra cranial stenosis documented by carotid Doppler study during transplant evaluation Modified Rankin Scale score of ≥ 2 or has any neurologic disability as confirmed by imaging (CT or MRI). Significant lower extremity peripheral vascular disease accompanied by rest pain or leg ulceration. Intolerant to anticoagulant or antiplatelet therapies or any other peri- or postoperative therapy that the investigator may administer based upon the patient's health status. Psychiatric disorder, or other psychosocial behavior that is likely to impair compliance with the study protocol. Receiving therapy with an investigational intervention or participating in any other clinical investigation at the time of enrollment. Condition, other than heart failure, that may limit survival to less than three (3) years and/or would exclude cardiac transplantation. Unwilling or unable to comply with any study requirement.
Facility Information:
Facility Name
University of California San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
University of Stanford
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
University of Miami
City
Coral Gables
State/Province
Florida
ZIP/Postal Code
33146
Country
United States
Facility Name
University of Chicago Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Facility Name
Indiana University Health, Inc. d/b/a Methodist Research Institute
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
St. Vincent Hospital & Health Care Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46260
Country
United States
Facility Name
Jewish Hospital
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
Facility Name
Minneapolis Heart Institute Foundation
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55407
Country
United States
Facility Name
Mayo Clinic Hospital - Saint Mary's Campus
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
CHI St. Luke's Baylor College of Medicine Medical Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Houston Methodist Hospital
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
University of Texas Health Science Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Providence Sacred Heart Hospital
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Clinical Trial to Evaluate the the ReliantHeart HeartAssist 5® VAD System in Patients Awaiting Heart Transplantation

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