Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System China Study(ATHENA)
Medtronic Cardiovascular
142 participants
Aug 26, 2026
INTERVENTIONAL
Conditions
Summary
To evaluate the safety and effectiveness of the Heli-FX EndoAnchor system in AAA subjects who without augmented radial fixation and/or sealing due to an endoleak or migration are at high risk for aneurysm-related complications or who are at high risk of migration or endoleak complications post-procedure, and to support product registration of Heli-FX EndoAnchor system with the National Medical Product Administration (NMPA) in China.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Subjects will be implanted with Heli-FX EndoAnchor System for AAA treatment
Locations(1)
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NCT07754318