NEXUS™ Aortic Arch Stent Graft System First In Man Study

Status Completed

Clinical Trial Summary

A multicenter, prospective, open-label, non-randomized, interventional clinical study, sponsored by Endospan Ltd. Patients will be followed-up for five years.

Clinical Trial Description

The purpose of the study is to evaluate the safety and performance of the Nexus™ Aortic Arch Stent Graft System for the endovascular treatment of thoracic aortic pathologies requiring landing in the Aortic Arch (zone 0, zone 1, zone 2). The Nexus™ Aortic Arch Stent Graft System is indicated for the endovascular treatment of thoracic aortic pathologies involving the aortic arch (such as aneurisms and dissections). The Nexus™ is intended to exclude the lesion from the blood circulation in patients diagnosed with thoracic aortic pathology and who have appropriate anatomy to accommodate the Nexus™ system in an endovascular procedure. The primary objectives of the study are to evaluate the safety and performance of the Nexus™ Aortic Arch Aneurysm Stent Graft System. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02365454
Study type	Interventional
Source	Endospan Ltd.
Contact
Status	Completed
Phase	N/A
Start date	August 2014
Completion date	June 2023

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