PRESERVE-Zenith® Iliac Branch System Clinical Extended Study
Trial ID or NCT#
NCT02571985
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
Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No
Inclusion Criteria:
- * An aortioiliac or iliac aneurysm* An unsuitable distal sealing site for a traditional Zenith iliac leg graft within the common lilac artery
Exclusion Criteria:
- * 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)
View on ClinicalTrials.gov
