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PRESERVE-Zenith® Branch Endovascular Graft-Iliac Bifurcation Clinical Study
Trial ID or NCT#
NCT02571907
Status
NOT RECRUITING
Purpose
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.
Official Title
Clinical Study to Evaluate the Safety and Effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation
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 - Pregnant, breast-feeding or planning on becoming pregnant prior to completion of the study - Unwilling or unable to comply with the follow-up schedule - Simultaneously participating in another investigative device or drug study
Investigator(s)
