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Study identifier: NCT07296744 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Pivotal Study of the SUpira System in Patients Undergoing High-Risk Percutaneous COronaRy InTervention (HRPCI)

Condition: Coronary Artery Disease · High Risk Percutaneous Coronary Intervention · Interventional Cardiology  ·  Sponsor: Supira Medical

PhaseNA
Planned participants358
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

The objective of this study is to assess the safety and efficacy of the Supira System in providing temporary cardiovascular hemodynamic support in patients undergoing HRPCI. Eligible patients will be randomized to undergo HRPCI with either the Supira System (investigational device) or the commercially available Impella systems (comparator device).

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

Talk to the study team

Supira Medical  ·  (669) 330-0883  ·  clinical@supiramedical.com

Chris DeMorrett  ·  669-330-0883

Always discuss trial participation with your own doctor first.

Locations (19)

Loma Linda University Medical CenterLoma Linda, California, United StatesNot Yet Recruiting
UC DavisSacramento, California, United StatesRecruiting
Los Robles Regional Medical CenterThousand Oaks, California, United StatesNot Yet Recruiting
Piedmont Heart InstituteAtlanta, Georgia, United StatesRecruiting
Emory University HospitalAtlanta, Georgia, United StatesNot Yet Recruiting
Northwestern UniversityChicago, Illinois, United StatesNot Yet Recruiting
Henry Ford Health / St. John HospitalDetroit, Michigan, United StatesRecruiting
CentraCareSaint Cloud, Minnesota, United StatesRecruiting
Washington University in St. LouisSt Louis, Missouri, United StatesRecruiting
University of Buffalo (Buffalo General)Buffalo, New York, United StatesRecruiting
Cuimc/NyphNew York, New York, United StatesRecruiting
Montefiore Medical CenterThe Bronx, New York, United StatesRecruiting

+ 7 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07296744