ViTAA Registry Pre- and Post-Operative Monitoring for Endovascular Aortic Aneurysm Repair and Serial Monitoring for AAA
Abdominal Aortic AneurysmsThis 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 HospitalToronto, Ontario
Canada
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UCGY - University of Calgary, Peter Lougheed Center
UCGY - University of Calgary, Peter Lougheed CenterCalgary, Alberta
Canada
Contact Study Team
CHUM - Centre Hospitalier de l'Université de Montréal
CHUM - Centre Hospitalier de l'Université de MontréalMontreal, Quebec
Canada
Contact Study Team
MUHC - McGill University Health Centre
MUHC - McGill University Health CentreMontréal, Quebec
Canada
Contact Study Team
- Study Sponsored By
- ViTAA Medical Solutions
- Participants Required
- More Information
- Study ID:
NCT05004051