Skip to content

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.

null

Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

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.

Lieu de l'étude

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

Contactez l'équipe d'étude

Primary Contact

Naomi Eisenberg

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

Contactez l'équipe d'étude

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

Contactez l'équipe d'étude

Primary Contact

Jennifer Satterthwaite

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

Contactez l'équipe d'étude

Primary Contact

Marie-Amélie Lukaszewski

[email protected]
(514) 934-1934
Étude parrainée par
ViTAA Medical Solutions
Participants recherchés
Plus d'informations
ID de l'étude: NCT05004051