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Evaluation of Adjunctive EndoAnchors for EVAR and TEVAR

NCT04100499 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2021-02-11

No results posted yet for this study

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)

Conditions

  • Aortic Aneurysm
  • Thoracic Aortic Aneurysm

Interventions

DEVICE

ESAR (Endosutured Aneurysm Repair)

EndoAnchors adjunctive therapy for EVAR and TEVAR

Sponsors & Collaborators

  • Hospital Universitario Ramon y Cajal

    lead OTHER

Principal Investigators

  • Andres Reyes Valdivia, Consultant · Vascular Surgery Department

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-31
Primary Completion
2020-12-31
Completion
2022-11-19
FDA Device
Yes

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04100499 on ClinicalTrials.gov