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RecruitingAbdominal Aortic Aneurysms

ViTAA Registry Pre- and Post-Operative Monitoring for Endovascular Aortic Aneurysm Repair and Serial Monitoring for AAA

Eligible age

18+ yrs

Accepts

All genders

Locations

4 states

Healthy volunteers

No

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About this study

This is a Prospective Registry study to collect imaging and clinical data both on patients with aortic aneurysm disease undergoing serial monitoring and on patients pre and post-endovascular repair, using ViTAA (The Sponsor) aortic mapping technology.

Sponsor: ViTAA Medical Solutions

You may qualify if…

  • ✓ 1. Patient is aged 18 years or over
  • ✓ 2. Infrarenal Aortic Aneurysm ≥ 45 mm in diameter.
  • ✓ 3. Patient meets on-IFU criteria for endovascular reconstruction

You may not qualify if…

  • ✕ 1. Patient has a known or clinically suspected major connective tissue disorder, autoimmune disorder, vasculitis, or aortic dissection.
  • ✕ 2. Patient has renal failure (defined as dialysis dependent or serum creatinine ≥2.0mg/dL or 175umol/L
  • ✕ 3. Patients with previous aortic reconstruction in the involved segment.
  • ✕ 4. Patients receiving oral or parenteral corticosteroid therapy for other unrelated disease. (Excludes inhaled corticosteroids).
  • ✕ 5. Patient has a sensitivity to contrast imaging agents.
  • ✕ 6. Patient has aortic dissection.
  • ✕ 7. Patient has atrial fibrillation.
  • ✕ 8. Patient has arrhythmia.

Where it's recruiting

Alabama

Birmingham

North Carolina

Chapel Hill

Washington

Seattle

Source: ClinicalTrials.gov · NCT05004051 · last updated 2025-09-19

ViTAA Registry Pre- and Post-Operative Monitoring for Endovascular Aor · TrialPath