The NEXUS™ Compassionate Use Data Collection Study

Status Completed

Clinical Trial Summary

A Multicenter, observational Data Collection Study to Evaluate the Safety and Performance of the Nexus™ Aortic Arch Stent Graft System in patients that were implanted with the device as part of Compassionate Use Procedures.

Clinical Trial Description

The purpose of the study is to collect and analyze data that is recorded as standard of care for patients that were implanted with the Nexus device as part of Compassionate Use Procedures.The data will be used to obtain additional information on the safety and performance of the Nexus™ Aortic Arch Stent Graft System in patients affected by pathologies involving the aortic arch. Data will be collected at each time point of patient's follow up conducted according to the standard of care in each site. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03420066
Study type	Observational
Source	Endospan Ltd.
Contact
Status	Completed
Phase
Start date	February 19, 2018
Completion date	November 28, 2023

View Details

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