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Study identifier: NCT07001332 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

ELEVATE High-Risk PCI Pivotal Study

Condition: High-Risk Percutaneous Coronary Intervention (High-risk PCI)  ·  Sponsor: Magenta Medical Ltd.

PhaseNA
Planned participants290
Who can joinAll sexes, 18 Years to 88 Years
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (33)

Banner-University Medical CenterPhoenix, Arizona, United StatesRecruiting
HonorHealth Scottsdale Shea Medical Center/HonorHealth Deer Valley Medical CenterScottsdale, Arizona, United StatesRecruiting
UC San Diego Medical CenterLa Jolla, California, United StatesRecruiting
University of California at San Francisco Medical Center/Zuckerberg San Francisco GeneralSan Francisco, California, United StatesRecruiting
Tampa General/USFTampa, Florida, United StatesRecruiting
Emory University Hospital / Emory University Hospital Midtown/ Emory Saint Joseph's HospitalAtlanta, Georgia, United StatesRecruiting
Wellstar Health SystemMarietta, Georgia, United StatesRecruiting
University of Illinois at ChicagoChicago, Illinois, United StatesRecruiting
University of Chicago Medical CenterChicago, Illinois, United StatesRecruiting
St. Elizabeth HealthcareEdgewood, Kentucky, United StatesRecruiting
Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Brigham & Women's HospitalBoston, Massachusetts, United StatesRecruiting

+ 21 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07001332