DyeVert™ Plus Contrast Reduction System Multicenter Observational Study

Status Completed

Clinical Trial Summary

This is a prospective, single arm, multi-center, observational clinical study of the DyeVert Plus System. The DyeVert Plus System is an FDA-cleared device designed to reduce contrast media volume delivered during angiography and permit real-time contrast media volume monitoring.

Clinical Trial Description

The purpose of this observational study is to evaluate the amount of contrast media saved using DyeVert Plus in coronary angiographic and/or interventional procedures performed with manual injection and evaluate the impact of predetermined thresholds and real-time monitoring. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03715452
Study type	Observational
Source	Osprey Medical, Inc
Contact
Status	Completed
Phase
Start date	July 1, 2017
Completion date	March 30, 2018

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