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Clinical Study to Collect Confirmatory Safety and Effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation
The purpose of this extended study is to collect confirmatory safety and effectiveness data on the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the commercially available Atrium iCAST™ covered stent in the treatment of aortoiliac and iliac aneurysms.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Mayo Foundation for Medical Education and Research
Phoenix, Arizona, United States
VA Palo Alto HCS
Palo Alto, California, United States
Stanford University Medical Center
Stanford, California, United States
Christine E. Lynn Heart and Vascular Institute
Boca Raton, Florida, United States
South Florida Medical Imaging
Fort Lauderdale, Florida, United States
University of Florida
Gainesville, Florida, United States
Emory University
Atlanta, Georgia, United States
St. Anthony's Medical Center
Rockford, Illinois, United States
Methodist Hospital of Indiana
Indianapolis, Indiana, United States
University of Kentucky Hospital
Lexington, Kentucky, United States
Last Updated
December 16, 2020
Zenith® Branch Endovascular Graft-Iliac Bifurcation,
DEVICE
Lead Sponsor
Cook Research Incorporated
NCT02577562
NCT00875563
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.
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