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Observational Registry Characterizing the CTAG Device With ACTIVE CONTROL — SURPASS  

Thoracic Diseases Clinical Trial

Official title:
Observational Registry Characterizing the Performance and Feature Use of the GORE® TAG® Conformable Thoracic Stent Graft Featuring ACTIVE CONTROL System

Clinical Trial Summary

Collect real-world clinical and device-specific outcomes of the GORE® TAG® Conformable Thoracic Stent Graft featuring ACTIVE CONTROL System (CTAG Device with ACTIVE CONTROL) in the treatment of aortic disease as part of routine clinical practice.

Clinical Trial Description

This is an observational, prospective, single-arm, post-market registry designed to collect real-world clinical and device specific outcomes of the GORE® TAG® Conformable Thoracic Stent Graft featuring ACTIVE CONTROL System (CTAG Device with ACTIVE CONTROL) in the treatment of aortic disease as part of routine clinical practice. A maximum of 20 clinical investigative sites in Europe will participate and up to 125 patients will be enrolled in this registry. All consecutive patients meeting protocol selection criteria, consented, with an intention to be treated with the CTAG Device with ACTIVE CONTROL will be included and followed through one year per institutional standard of care. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03286400
Study type Observational [Patient Registry]
Source W.L.Gore & Associates
Contact
Status Completed
Phase
Start date October 18, 2017
Completion date October 9, 2019
View Details
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