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Assessment of Catheter-based Interrogation and Standard Techniques for Fractional Flow Reserve Measurement: the ACIST-FFR Study
This study will assess the differences between Fractional Flow Reserve (FFR) measurements made by the Navvus catheter and a commercially available pressure guidewire in up to 240 subjects where FFR is clinically indicated. All subjects will receive diagnostic treatment according to clinical indications and center standard practice.
The ACIST-FFR study is a prospective, open label, observational, multi-center study designed to assess the differences, if any, between FFR measured by the Navvus catheter and a commercially available 0.014-inch pressure guidewire (St. Jude Medical, Volcano, hereafter referred to as the PW) in subjects with coronary artery disease (CAD) undergoing coronary angiography. This will be accomplished by comparing the FFR measurement obtained with the ACIST Medical Systems RXi System and Navvus catheter with the FFR measurement obtained by using a PW within the same subject across the same target lesion at the same time.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Scripps Green Hospital
La Jolla, California, United States
Long Beach VA Medical Center
Long Beach, California, United States
Stanford School of Medicine
Stanford, California, United States
Medstart Washington Hospital Center
Washington D.C., District of Columbia, United States
University of Chicago Medicine
Chicago, Illinois, United States
Iowa Heart Center
West Des Moines, Iowa, United States
Metropolitan Cardiology Heart and Vascular Institute
Minneapolis, Minnesota, United States
University of Minnesota
Minneapolis, Minnesota, United States
Saint Louis University
St Louis, Missouri, United States
Columbia University Medical Center / New York Presbyterian Hospital
New York, New York, United States
Start Date
November 1, 2015
Primary Completion Date
January 1, 2017
Completion Date
January 1, 2017
Last Updated
December 6, 2016
240
ESTIMATED participants
RXi System
DEVICE
Pressure Wire
DEVICE
Lead Sponsor
Acist Medical Systems
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.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT01311323