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The Enzen Trial: Comparison of Evar Endoprosthesis: Endurant Versus Zenith (ENZEN)

H

Hospital do Servidor Publico Estadual

Status

Active, not recruiting

Conditions

Aortoiliac Atherosclerosis
Aortic Aneurysm

Treatments

Device: EVAR

Study type

Observational

Funder types

Other

Identifiers

NCT05969782
32380920.5.0000.5463

Details and patient eligibility

About

A prospective, non-randomized trial of patients submitted to EVAR for aortoiliac aneursym using Endurant II (Medtronic) or Zenith (Cook).

Full description

A prospective, non-randomized trial of patients submitted to EVAR for aortoiliac aneursym using Endurant II (Medtronic) or Zenith (Cook).

The patients will be evaluated in a follow-up, regarding overall mortality rate, perioperative mortality rate and outcomes, such as Endoleaks and reinterventions.

Enrollment

100 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Aortoiliac infra-renal aneurysms.

Exclusion Criteria: Thoracoabdominal aortic aneurysms, pararenal and supra-renal aortic aneurysms

  • Patients not suitable for EVAR.

Trial design

100 participants in 2 patient groups

Endurant II
Description:
Patients with aortoiliac aneurysm submitted to EVAR with Endurant II.
Treatment:
Device: EVAR
Zenith
Description:
Patients with aortoiliac aneurysm submitted to EVAR with Zenith.
Treatment:
Device: EVAR

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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