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

Abdominal Aortic Aneurysms

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.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

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

Exclusion Criteria:

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.

Study Location

UHN - University Health Network - Toronto General Hospital
UHN - University Health Network - Toronto General Hospital
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Naomi Eisenberg

[email protected]
UCGY - University of Calgary, Peter Lougheed Center
UCGY - University of Calgary, Peter Lougheed Center
Calgary, Alberta
Canada

Contact Study Team

Primary Contact

Emi Sanders

[email protected]
CHUM - Centre Hospitalier de l'Université de Montréal
CHUM - Centre Hospitalier de l'Université de Montréal
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Jennifer Satterthwaite

[email protected]
514 890-8000
MUHC - McGill University Health Centre
MUHC - McGill University Health Centre
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

Marie-Amélie Lukaszewski

[email protected]
(514) 934-1934
Study Sponsored By
ViTAA Medical Solutions
Participants Required
More Information
Study ID: NCT05004051