Recruiting

Jarvik 2000

Sponsor:

Jarvik Heart, Inc.

Code:

NCT01627821

Conditions

Heart Failure

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Jarvik 2000 VAS

HeartMate II

Study Details

Brief summary:

This investigation will be conducted as an interventional intention-to-treat clinical study in a population of end stage heart failure patients who meet specific inclusion and exclusion criteria. The multi-center study will be prospective, dual-armed, non-blinded (open-label) and randomized, comparing a treatment group receiving the Jarvik 2000 LVAS with Post-Auricular Connector to an active control group treated with the PMA approved Thoratec HeartMate® II LVAS for Destination Therapy.

Conditions

Heart Failure

Study ID

NCT01627821

Start date

Feb, 2013

Status verified date

Mar, 2024

Completion date

Mar, 2025

Anticipated

Primary completion date

Mar, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Cardiac transplantation ineligible.
2. Late stage heart failure in NYHA Class IIIb or IV for at least 45 of past 60 days.
3. Cardiac Index < 2.2 L / min / m2
4. LVEF = 25% or less
5. Patients on Optimal Medical Management (OMM) as defined in Section 9.2 OR dependent on intra-aortic balloon counter-pulsation for 7 days OR other temporary (indicated for 30 days use, or less) mechanical circulatory support for 7 days, OR supported with IV inotropes for 7 days and failing to respond.
6. BSA > 1.2 m2 and < 2.5 m2.

Exclusion Criteria:

1. History of cardiac transplantation or left ventricular reduction procedure.
2. Clinical conditions, other than heart failure, which could limit survival to less than three years.
3. Cause of heart failure due to, or associated with, uncorrected thyroid disease, obstructive / restrictive cardiomyopathy, pericardial disease, amyloidosis, dermatomyositis, or active myocarditis.
4. Intolerance to anti-coagulation or anti-aggregation therapy required for post-operative therapy.
5. Known sensitivity to products of bovine origin. The Jarvik 2000 incorporates a Hemashield vascular graft. Patients with a known sensitivity to products of bovine origin should not be implanted.
6. Chronic immunosuppression.

Study Design

Enrollment

350 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Jarvik 2000 Treatment

Jarvik 2000 VAS, Post-Auricular Cable

active comparator: HeartMate II Control

HeartMate II VAS Control

Interventions

Jarvik 2000 VAS

Jarvik 2000 LVAD

HeartMate II

HeartMate II LVAD

Primary outcome measure

  • Non-inferiority to Control Group. [ Time Frame: 2 years ]

Central Contacts and Locations

Central contacts

Locations

Columbia/NY Presbyterian

Recruiting

New York, New York, United States, 10032

Contacts

Yoshifumi Naka, MD PhD

212-305-0828

More Information

Sponsor

Jarvik Heart, Inc.

Last update posted

Mar 20, 2024

Last verified

Mar, 2024

Keywords

  • Heart Failure

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Jarvik Heart, Inc. on 2024-03-20.