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

Abdominal Aortic Aneurysms Clinical Trial

Official title:
Prospective Registry Study to Collect Imaging and Clinical Data on Patients With Aortic Aneurysm Disease Undergoing Serial Monitoring & Pre and Post Endovascular Repair

Clinical Trial Summary

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.

Clinical Trial Description

This a prospective, multi-center, registry of patients that are being assessed with the ViTAA software. Patients will be enrolled at selected North American centers in the US and Canada. The Registry will enroll patients from the following two populations: - patients who are scheduled and ultimately receive endovascular infrarenal aortic aneurysm repair (EVAR); - patients who do not yet qualify for infrarenal aortic aneurysm repair based on anatomic size criteria who are enrolled in a serial monitoring program. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05004051
Study type Observational [Patient Registry]
Source ViTAA Medical Solutions
Contact Denis Bilodeau
Phone 5145728673
Email denisbilodeau@vitaamedical.com
Status Recruiting
Phase
Start date December 15, 2021
Completion date December 31, 2026
View Details
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