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Clinical Trials/NCT00281411
NCT00281411
Completed
Not Applicable

Follow-up Study of Endovascular Abdominal Aortic Aneurysm Treatment

Clinical Research Office Imaging Division1 site in 1 country46 target enrollmentMarch 2001

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aortic Aneurysm, Abdominal
Sponsor
Clinical Research Office Imaging Division
Enrollment
46
Locations
1
Status
Completed
Last Updated
8 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 2001
End Date
March 2009
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Clinical Research Office Imaging Division
Responsible Party
Sponsor Investigator
Principal Investigator

Clinical Research Office Imaging Division

Clinical research coordinator

UMC Utrecht

Eligibility Criteria

Inclusion Criteria

  • Patient is planned for endovascular abdominal aortic aneurysm repair

Exclusion Criteria

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

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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