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PRESERVE-Zenith® Iliac Branch System Clinical Extended Study
Trial ID or NCT#
Status
NOT RECRUITING
Purpose
The PRESERVE-Zenith® Iliac Branch System Clinical Study is a clinical trial to collect confirmatory safety and effectiveness data on the Zenith® Branch Endovascular Graft-Iliac Bifurcation System. This system is made up of two devices: the Zenith® Branch Endovascular Graft-Iliac Bifurcation and the ConnectSX™ covered stent in the treatment of aorto-iliac and iliac aneurysms
Official Title
Clinical Study to Evaluate the Safety and Effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation With the ConnectSX™
Eligibility Criteria
- - An aortioiliac or iliac aneurysm - An unsuitable distal sealing site for a traditional Zenith iliac leg graft within the common lilac artery
- - Less than 18 years of age - Inability or refusal to give informed consent - Disease considerations that would compromise patient safety or study outcomes - Unsuitable arterial anatomy
Investigator(s)
