Actively Recruiting

Age: 18Years +
All Genders
NCT06866769

Efficacy of Biomarkers and CEUS Versus CTA in AAA Follow-up Post-EVAR

Led by Instituto de Investigacion Sanitaria La Fe · Updated on 2025-03-10

60

Participants Needed

1

Research Sites

196 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective observational study evaluates the efficacy of contrast-enhanced ultrasound and biomarker determination in the follow-up of patients with abdominal aortic aneurysm (AAA) treated with Endovascular Aneurysm Repair (EVAR). Currently, computed tomography angiography (CTA) is the standard for follow-up, although it has disadvantages such as radiation exposure and the use of iodinated contrasts. Contrast-enhanced ultrasound (CEUS), free of radiation and nephrotoxicity, and biomarkers could reduce the need for CTA minimizing the associated risks. Biomarkers will be measured before and after EVAR and CEUS will be performed at various time points and compared with CTA results to validate concordance and effectiveness in detecting endoleaks and aneurysm remodeling. The objectives include determining the efficacy of these combined methods and establishing a follow-up protocol that reduces exposure to radiation and iodinated contrast agents.

CONDITIONS

Official Title

Efficacy of Biomarkers and CEUS Versus CTA in AAA Follow-up Post-EVAR

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with abdominal aortic aneurysm under follow-up who will be treated with Endovascular Aneurysm Repair (EVAR)
  • Signed informed consent for CT angiography, contrast-enhanced ultrasound, and biomarker testing
Not Eligible

You will not qualify if you...

  • Patients with inflammatory abdominal aortic aneurysms
  • Patients with ruptured abdominal aortic aneurysms

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospital La Fe

Valencia, Valencia, Spain, 46026

Actively Recruiting

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Research Team

J

Juan Manuel Sanchís García

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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