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ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registry) — ANCHOR  

Aortic Aneurysm Clinical Trial

Official title:
Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registry

Clinical Trial Summary

The ANCHOR registry is a multi-center, post-market, non-interventional, non-randomized, prospective study. Subjects must sign an ICF prior to obtaining any study specific information. Subjects are eligible to be consented up to 30 days post-procedure. Enrolled subjects will be followed as per local 'standard of care' for up to 5 years post procedure. Study recommended follow-up is per SVS and ESVS guidance.

Clinical Trial Description

The objective of the ANCHOR registry is to expand the clinical knowledge based on the use of the Heli-FX™ EndoAnchor™ System. This registry will include "real world" use over a broad spectrum of geographies, by a wide variety of practicing clinicians, and with a minimal degree of subject selection criteria. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01534819
Study type Observational
Source Medtronic Cardiovascular
Contact
Status Active, not recruiting
Phase
Start date April 2012
Completion date December 3, 2025
View Details
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