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Clinical Trial Summary

This is a single-center study to evaluate the safety and effectiveness of three investigational devices, the Cook Custom Aortic Endograft, the Zenith t-Branch Endovascular Graft, and the Surgeon-Modified Endografts in the treatment of aortic pathologies involving the visceral vessels. The three investigational devices offer an endovascular approach to treat complex aortic pathologies that cannot be treated with commercially available devices. This customized, endovascular approach has the potential to decrease hospital length of stay, pulmonary complications, and in-hospital mortality.


Clinical Trial Description

Once the participant has signed the approved informed consent the following tests will be done to determine final subject eligibility and which device will be used: Clinical Exam, Blood Tests, CT Scans (with and without contrast), Abdominal Device X-ray, and Angiography. The participants will be followed for 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02043691
Study type Interventional
Source University of Alabama at Birmingham
Contact Adam W Beck, MD
Email awbeck@uabmc.edu
Status Recruiting
Phase N/A
Start date June 2014
Completion date October 2027

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