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Clinical Trial Summary

EndoAnchors (Heli-FX device, Medtronic, Santa Rosa) have beed described to improve fixation (mimicking an open surgical anastomosis) during or after EVAR/TEVAR. The investigators want to describe the outcomes of all consecutive patients treated with this device (retrospective and prospective data - observational study)


Clinical Trial Description

EndoAnchors (Heli-FX device, Medtronic, Santa Rosa) have beed designed to improve the Endovascular aortic repair. This device is described to mimic an open surgical anastomosis during or after EVAR/TEVAR. The investigators want to describe the outcomes of all consecutive patients treated with this device (retrospective and prospective data - observational study), these outcomes will be described in terms of type IA Endoleaks, migration and sac regression. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04100499
Study type Observational [Patient Registry]
Source Hospital Universitario Ramon y Cajal
Contact Andres Reyes Valdivia, Consultant
Phone +34629586239
Email cauzaza@hotmail.com
Status Recruiting
Phase
Start date December 31, 2019
Completion date November 19, 2022

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