Aortic Aneurysm, Abdominal Clinical Trial
Official title:
Inflammation and Risk Prediction in Patients With Abdominal Aortic Aneurysm
Verified date | April 2017 |
Source | Vanderbilt University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to better understand the role of inflammation in the pathophysiology of abdominal aortic aneurysm. In this study we hope to show better ways of predicting risk in this condition by using a combination of FDG-PET with CT.
Status | Completed |
Enrollment | 14 |
Est. completion date | February 2014 |
Est. primary completion date | July 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with AAA between 3 to 5 cm - Patients with AAA > 5cm in whom the risk of operative intervention is prohibitive in the opinion of the surgeon. - No allergies to iodinated contrast. - Diabetic patients will be eligible for this study. Patient on metformin will be asked not to take the drug for one day prior to and for two days after the procedure. - Subjects must be able to give informed consent Exclusion Criteria: - Patients with an impaired kidney function, significantly elevated creatinine levels after angiography/PCI (serum creatinine level >1.5 mg/dl) will be excluded form the study. - Unstable patients or those with decompensated heart failure will be excluded because of safety reasons. - Pregnant or lactating women will be excluded. Pregnancy will need to be tested in all pre-menopausal women. |
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt University Medical Center | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Give more details that may enable us to better assess the chance of AAA expansion or rupture | 2 Years |
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