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

Authors
Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2012
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.
Epistemonikos ID: ad20afb2ab98b82c6aea1b52b5440a11eb1171bd
First added on: May 10, 2024