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AVERT™ Clinical Trial
The Osprey Medical AVERT System is indicated to reduce contrast media (CM) exposure to the kidneys during percutaneous coronary procedures thereby reducing the risk of contrast induced nephropathy (CIN).
The purpose of this trial is to assess the AVERT System device, which is designed to limit the volume of CM (Contrast Media) utilized, during a staged therapeutic coronary PCI (Percutaneous Coronary Intervention) or a coronary diagnostic procedure that is anticipated to become a PCI (i.e. ad hoc PCI) for the reduction of CIN (Contrast Induced Nephropathy).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
UCSD Medical Center
La Jolla, California, United States
Long Beach CA VA Hospital
Long Beach, California, United States
Kaiser Permanente Los Angeles Medical Center
Los Angeles, California, United States
Stanford Hospital and Clinics
Stanford, California, United States
Harbor UCLA Medical Center
Torrance, California, United States
The Heart & Vascular Institute of Florida
Clearwater, Florida, United States
University of FL College of Medicine - Jacksonville
Jacksonville, Florida, United States
St. Vincent's Ambulatory Care (dba St. Vincent's Cardiology)
Jacksonville, Florida, United States
Tallahassee Research Institute, Inc.
Tallahassee, Florida, United States
Emory University Hospital Midtown
Atlanta, Georgia, United States
Start Date
December 1, 2013
Primary Completion Date
July 1, 2015
Completion Date
September 1, 2015
Last Updated
February 28, 2017
578
ACTUAL participants
AVERT
DEVICE
Lead Sponsor
Osprey Medical, Inc
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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