PRESERVE-Zenith® Iliac Branch System Clinical Extended Study

Cook Group

Status

Conditions: Aorto-iliac Aneurysms; Iliac Aneurysms

Treatments: Device: Zenith® Branch Endovascular Graft-Iliac Bifurcation System

Study type: Expanded Access

Funder types: Industry

Identifiers

NCT02571985

05-625 CA-P1

Details and patient eligibility

About

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

Sex: All

Ages: 18+ years old

Volunteers: No 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