Recruiting

Elevate LVAD

Sponsor:

Magenta Medical Ltd.

Code:

NCT07001332

Conditions

High-Risk Percutaneous Coronary Intervention (High-risk PCI)

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Elevate

Impella

Study Details

Brief summary:

The ELEVATE III Pivotal Study is a prospective, multi-center, open-label, interventional, randomized, controlled study with an active control group. The study is intended to assess the safety and efficacy of the Elevate™ percutaneous Left Ventricular Assist Device System in patients referred to high-risk percutaneous coronary interventions (HR-PCI).

Conditions

High-Risk Percutaneous Coronary Intervention (High-risk PCI)

Study ID

NCT07001332

Start date

Jul 25, 2025

Status verified date

Jul, 2026

Completion date

Sep 16, 2027

Anticipated

Primary completion date

Mar 16, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Non-emergent, percutaneous coronary intervention is planned on at least one stenotic lesion of a native coronary artery or bypass graft (de novo or restenosis).
2. A heart team that includes an interventional cardiologist and cardiac surgeon has determined that HR- PCI is an appropriate therapeutic option.
3. Participant signed the informed consent.

Exclusion Criteria:

1. Cardiogenic shock or acutely decompensated pre-existing chronic heart failure.
2. Prior stroke with any permanent, significant (mRS>2) neurological deficit, or stroke or TIA within 3 months prior to enrollment.
3. Any condition or scheduled surgery that will require discontinuation of the antiplatelet and/or anticoagulation therapy within 90 days of the index procedure.
4. Evidence of left ventricular thrombus.
5. Aortic valve stenosis/calcification (valve area ≤ 1.5 cm2).
6. ≥ Moderate aortic valve regurgitation (≥ 2+ on a 4-grade scale by transthoracic echocardiography).
7. Femoral access site incompatibility that precludes placement of either the Treatment or Control device.
8. Patient on dialysis.
9. Known or suspected coagulopathy OR abnormal coagulation parameters.
10. Known allergy, sensitivity or intolerance to nickel.
11. Infection of the proposed procedural access site; OR suspected systemic active infection, including any fever or known active COVID-19 infection.
12. Allergy, sensitivity or intolerance to heparin, or contrast media, including known heparin-induced thrombocytopenia (HIT).
13. Any non-cardiac condition with a life expectancy < 12 months.
14. Subject participation in another investigational drug or device trial (with the exception of post-market registries and observational studies, subject to Sponsor review and approval).
15. Pregnancy or breast-feeding.
16. Subject has other medical, social, or psychological problems that, in the opinion of the Investigator, compromise the participant's ability to provide written informed consent and/or to comply with study procedures.
17. Subject belongs to a vulnerable population.

Study Design

Enrollment

290 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Elevate

Subjects receiving the Elevate System

active comparator: Impella

Subjects receiving the Impella System

Interventions

Elevate

The Elevate System is a catheter- mounted, self-expanding and retrievable, continuous-flow pump, designed to unload the left ventricle by actively transporting blood from the left ventricle into the ascending aorta, thus augmenting cardiac output and maintaining systemic arterial pressure during complex/high-risk coronary interventions. Subjects will receive an Elevate prior to their high-risk percutaneous intervention.

Impella

Subjects will receive an Impella prior to their high-risk percutaneous intervention.

Primary outcome measure

  • A composite of the incidence of major safety and effectiveness parameters. [ Time Frame: 30 days ]

Central Contacts and Locations

Locations

Banner-University Medical Center

Recruiting

Phoenix, Arizona, United States, 85006

Contacts

Principal Investigator:

David G Rizik, MD

HonorHealth Scottsdale Shea Medical Center/HonorHealth Deer Valley Medical Center

Recruiting

Scottsdale, Arizona, United States, 85260

Contacts

Principal Investigator:

Taral Patel, MD

UC San Diego Medical Center

Recruiting

La Jolla, California, United States, 92093

Contacts

Principal Investigator:

Ehtisham Mahmud, MD

University of California at San Francisco Medical Center/Zuckerberg San Francisco General

Recruiting

San Francisco, California, United States, 94143

Contacts

Principal Investigator:

Krishan Soni, MD

Tampa General/USF

Recruiting

Tampa, Florida, United States, 33606

Contacts

Emory University Hospital / Emory University Hospital Midtown/ Emory Saint Joseph's Hospital

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

William Nicholson, MD

717-817-7233wjnicho@emory.edu

Principal Investigator:

William Nicholson, MD

Wellstar Health System

Recruiting

Marietta, Georgia, United States, 30062

Contacts

University of Illinois at Chicago

Recruiting

Chicago, Illinois, United States, 60612

Contacts

Principal Investigator:

Adhir R Shroff, MD

University of Chicago Medical Center

Recruiting

Chicago, Illinois, United States, 60637

Contacts

Principal Investigator:

Sandeep Nathan, MD

St. Elizabeth Healthcare

Recruiting

Edgewood, Kentucky, United States, 41017

Contacts

Massachusetts General Hospital

Recruiting

Boston, Massachusetts, United States, 02114

Contacts

Suzanne J Baron, MD

617-643-9617sbaron@mgb.org

Brigham & Women's Hospital

Recruiting

Boston, Massachusetts, United States, 02115

Contacts

Principal Investigator:

Ajar Kochar, MD

Boston Medical Center

Recruiting

Boston, Massachusetts, United States, 02118

Contacts

Principal Investigator:

Nir Ayalon, MD

Beth Israel Deaconess Medical Center

Recruiting

Boston, Massachusetts, United States, 02215

Contacts

Principal Investigator:

Robert Yeh, MD

UMass Memorial Medical Center

Recruiting

Worcester, Massachusetts, United States, 01605

Contacts

Principal Investigator:

Nikolaos Kakouros, MD

Henry Ford Health

Recruiting

Detroit, Michigan, United States, 48202

Contacts

Minneapolis Heart Institute

Recruiting

Minneapolis, Minnesota, United States, 55407

Contacts

St. Luke's Hospital of Kansas City

Recruiting

Kansas City, Missouri, United States, 64111

Contacts

Principal Investigator:

Dany Jacob, MD

Atlantic Health System

Recruiting

Morristown, New Jersey, United States, 07960

Contacts

Principal Investigator:

Saad Ahmad, MD

Robert Wood Johnson University Hospital

Recruiting

New Brunswick, New Jersey, United States, 08901

Contacts

Principal Investigator:

Tudor Vagaonescu, MD

Maimonides Health

Recruiting

Brooklyn, New York, United States, 11219

Contacts

Buffalo General Medical Center

Recruiting

Buffalo, New York, United States, 14203

Contacts

Principal Investigator:

Vijay Iyer, MD

Northwell Health

Recruiting

Manhasset, New York, United States, 11030

Contacts

NYU Langone/Bellevue/Long Island

Recruiting

New York, New York, United States, 10023

Contacts

Principal Investigator:

Dimitrios Bliagos, MD

Mount Sinai

Recruiting

New York, New York, United States, 10029

Contacts

Columbia University Medical Center/NYPH

Recruiting

New York, New York, United States, 10032

Contacts

Weill Cornell Medical Center

Recruiting

New York, New York, United States, 10065

Contacts

Mercy Health

Recruiting

Cincinnati, Ohio, United States, 45211

Contacts

Principal Investigator:

Adam Raskin, MD

Kaiser Permanente

Recruiting

Clackamas, Oregon, United States, 97015

Contacts

Principal Investigator:

Jeffrey A Marbach, MD

TriStar Centennial Medical Center

Recruiting

Nashville, Tennessee, United States, 37203

Contacts

Principal Investigator:

Brian Jefferson, MD

Inova Schar Heart & Vascular

Recruiting

Falls Church, Virginia, United States, 22042

Contacts

Principal Investigator:

Shashank Sinha, MD

Swedish Cherry Hill

Recruiting

Seattle, Washington, United States, 98122

Contacts

Principal Investigator:

Christopher Brown, MD

Advocate Aurora Health Research Institute- St. Luke's Medical Center

Recruiting

Milwaukee, Wisconsin, United States, 53215

Contacts

More Information

Sponsor

Magenta Medical Ltd.

Last update posted

Jul 16, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Magenta Medical Ltd. on 2026-07-16.