Feasibility Study SA of the Supira System for HRPCI

Status Not yet recruiting

Clinical Trial Summary

The objective is to assess the feasibility and safety of the Supira System in providing temporary cardiovascular hemodynamic support in patients undergoing HRPCI.

Clinical Trial Description

The Feasibility Study SA is planned as a prospective, single-arm, interventional multi-center study enrolling up to 30 subjects. The Supira Catheter is a single-use percutaneous expandable blood pump designed to unload the left ventricle by actively transporting blood from the left ventricle into the aorta. The Supira System is a temporary ventricular support device indicated for use for a short time during high-risk percutaneous coronary interventions (PCI) performed electively or urgently in hemodynamically stable patients, with severe coronary artery disease. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05864248
Study type	Interventional
Source	Supira Medical
Contact	Nicole Haratani
Phone	(408) 560-2500
Email	nicole@supiramedical.com
Status	Not yet recruiting
Phase	N/A
Start date	June 1, 2023
Completion date	February 28, 2024

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