Endovascular Exclusion of Abdominal Aortic Aneurysms in High Risk Patients

Completed · Not applicable

Conditions studied: Abdominal Aortic Aneurysm, Iliac Aneurysm, Internal Iliac Aneurysm

In brief

The purpose of this study is to assess the role of abdominal aneurysm and iliac aneurysm exclusion using an endovascular prosthesis.

Key facts

Study ID

NCT00583414

Run by

The Cleveland Clinic

People needed

401

Starts

1998-09-01

Expected to finish

2017-10-01

Last updated by the study team

2019-01-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The aneurysm is >/= 5 cm or larger, or with a high risk of rupture due to its shape, history of growth, symptoms, or the presence of a large (>2 cm) iliac aneurysm
• Anticipated mortality greater than 10 percent with conventional surgery
• Life expectancy greater than 2 years
• Suitable arterial anatomy
• Absence of systemic disease or allergy that precludes an endovascular repair
• Capable of giving informed consent and willingness to comply with the follow-up schedule

You may not qualify if…

• Pregnancy
• History of anaphylactic reaction to contrast material with an inability to properly prophylax the patient appropriately
• Allergy to stainless steel or polyester
• Unwilling to comply with the follow-up schedule
• Serious or systemic groin infection
• Coagulopathy, other than coumadin therapy
• Inability to give informed consent

Where it is running

• Cleveland Clinic — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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