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No Longer AvailableNCT02475798

PRESERVE-Zenith® Branch Endovascular Graft-Iliac Bifurcation

Clinical Study to Collect Confirmatory Safety and Effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation

Status
No Longer Available
Phase
—
Study type
Expanded Access
Enrollment
—
Sponsor
Cook Research Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEZenith® Branch Endovascular Graft-Iliac Bifurcation,Implantation of the following devices: Zenith® Branch Endovascular Graft-Iliac Bifurcation, the Atrium iCAST™, and the Zenith® Flex AAA Endovascular Graft.

Timeline

First posted
2015-06-19
Last updated
2020-12-16

Locations

26 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02475798. Inclusion in this directory is not an endorsement.

PRESERVE-Zenith® Branch Endovascular Graft-Iliac Bifurcation (NCT02475798) · Clinical Trials Directory