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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02463760
Other study ID # 150023
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2015
Est. completion date February 14, 2022

Study information

Verified date March 2022
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to investigate imaging findings, which can help us to predict factors contributing to abdominal aortic aneurysm growth and rupture.


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date February 14, 2022
Est. primary completion date February 14, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Individuals between 18 and 80 years old receiving medical care at University of Minnesota Medical Center who have a normal aorta CTA within the previous year - Or patients with known AAA with growth rate of 0-0.2 cm/year - Or patients with known AAA with growth rate of greater than 0.5 cm/year. Exclusion Criteria: - Subjects with ferromagnetic implants - Penile implant - Hip replacement - History of shrapnel or shot gun injury - Body mass index = 30 - Cardiac pacemakers - Severe claustrophobia - Large tattoos on the torso

Study Design


Intervention

Other:
Medical imaging


Locations

Country Name City State
United States University of Minnesota Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Imaging findings correlating with abdominal aortic aneurysm growth and rupture 1 year
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