Feasibility Study of the Intravascular Ventricular Assist System (iVAS)

Status Recruiting

Clinical Trial Summary

The purpose of this feasibility study is to assess the preliminary safety and clinical performance of the intravascular ventricular assist system (iVAS).

Clinical Trial Description

This is a single-arm, non-randomized study designed to assess the preliminary safety and clinical performance of the NuPulseCV iVAS.

Data obtained from the study will be used to make device modifications, refine the patient population, and inform the design a future clinical trial suitable for assessing longer-term use in heart failure patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02645539
Study type	Interventional
Source	NuPulseCV
Contact	Lori Rhoten
Phone	1-800-216-1778
Email	CTT@nupulsecv.com
Status	Recruiting
Phase	N/A
Start date	April 2016
Completion date	December 2020

View Details

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