PRESERVE-Zenith® Iliac Branch System Clinical Extended Study

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

Status

NO_LONGER_AVAILABLE

Phases

Unknown

Study type

Expanded Access

Source

ClinicalTrials.gov

Registry ID

NCT02571985

Enrollment

Unknown

Registered

2015-10-08

Start date

2012-05-31

Completion date

2017-10-31

Last updated

2017-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aorto-iliac Aneurysms, Iliac Aneurysms

Keywords

Zenith aortoiliac aneurysm, iliac aneurysm, branch, connections, endovascular graft, graft-iliac bifurcation, Aneurysm, Vascular Diseases, Cardiovascular Diseases

Brief summary

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

Interventions

DEVICEZenith® Branch Endovascular Graft-Iliac Bifurcation System

Zenith® Branch Endovascular Graft-Iliac Bifurcation (Branch Graft) with the ConnectSX™

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026