NCT02571907

PRESERVE-Zenith® Branch Endovascular Graft-Iliac Bifurcation Clinical Study

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

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Cook Research Incorporated · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this extended study is to evaluate the safety and effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the commercially available Atrium iCAST™ covered stent in patients in a treatment of aortoiliac and iliac aneurysms.

Conditions

• Aortoiliac Aneurysms
• Iliac Aneurysms

Interventions

Type	Name	Description
DEVICE	Zenith® Branch Endovascular Graft-Iliac Bifurcation,	Implantation of the Zenith® Branch Endovascular Graft-Iliac Bifurcation.
DEVICE	Atrium iCAST™	Implantation of Atrium iCAST
DEVICE	Zenith® Flex AAA Endovascular Graft	Implantation of the Zenith Flex Endovascular Graft

Timeline

• Start date: 2014-04-01
• Primary completion: 2015-11-01
• Completion: 2020-11-04
• First posted: 2015-10-08
• Last updated: 2025-07-16
• Results posted: 2025-07-16

Locations

28 sites across 1 country: United States

Regulatory

• FDA-regulated device study