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PRESERVE-Zenith® Iliac Branch System Clinical Extended Study

NCT02571985 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2017-03-07

No results posted yet for this study

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

Conditions

  • Aorto-iliac Aneurysms
  • Iliac Aneurysms

Interventions

DEVICE

Zenith® Branch Endovascular Graft-Iliac Bifurcation System

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

Sponsors & Collaborators

  • Cook Group Incorporated

    lead INDUSTRY

Principal Investigators

  • W. Anthony Lee, MD FACS · Christine E. Lynn Heart and Vascular Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2013-04-30
Completion
2017-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02571985 on ClinicalTrials.gov