Skip to content

Follow-up of Endovascular Aneurysm Treatment - The FEAT Trial

Follow-up Study of Endovascular Abdominal Aortic Aneurysm Treatment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00281411
Enrollment
46
Registered
2006-01-24
Start date
2001-03-31
Completion date
2009-03-31
Last updated
2018-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Aneurysm, Abdominal

Keywords

Blood Vessel Prosthesis Implantation, Endovascular aneurysm repair, Magnetic Resonance Angiography, Computed Tomography Angiography, Endoleak

Brief summary

After endovascular abdominal aortic aneurysm repair, life-long follow-up is needed to monitor the effectiveness of exclusion of the aneurysm sac from blood flow. For this reason, aneurysm diameter and the presence of endoleaks is evaluated with CT angiography yearly after Endovascular Aneurysm Repair (EVAR). The aim of this study is to investigate the value of MRA examinations for the follow-up of these patients. The advantages of MRA with respect to CTA are no use of ionizing radiation, use of less nephrotoxic contrast agents.

Detailed description

The FEAT trial (Follow-up of Endovascular Aneurysm Treatment) is designed as a prospective, single-center, follow-up study. 100 Patients will be enrolled in this study. These patients will undergo additional MRA-examinations the day before EVAR, the day after EVAR, 6 months and 1 year after EVAR. These patients also participate in the conventional CTA follow-up scheme which comprises a pre- and post-operative CTA and a CTA yearly thereafter. Coagulation parameters in the blood will be measured before and 1 year after EVAR.

Interventions

Computed Tomography Angiography

PROCEDUREMagnetic Resonance Angiography

Magnetic Resonance Angiography

Sponsors

Clinical Research Office Imaging Division
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patient is planned for endovascular abdominal aortic aneurysm repair

Exclusion criteria

* contraindication for MRI examination * claustrophobia * pacemaker * other non-MRI compatible implants

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026