Carotid Artery Disease - ACT
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Trial Sponsor
Abbott Vascular
Principal Investigator
Gregory J. Mishkel, MD
Trial Name
Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects Who Are at Standard Risk for Carotid Endarterectomy With Significant Extracranial Carotid Stenotic Disease (ACT I)
Purpose
The study is being conducted to demonstrate the non-inferiority of carotid artery stenting (CAS) using the Emboshield® Embolic Protection System and Emboshield® Pro Embolic Protection System with the Xact® Carotid Stent System to carotid endarterectomy (CEA) for the treatment of asymptomatic extracranial carotid atherosclerotic disease.
Details
Patients will be randomized to either an interventional treatment using a carotid artery stent and filter or the surgical procedure of carotid endarterectomy, on a 3:1 basis. This means that three interventional procedures will be conducted to each surgical (CEA) one, on average, for every four patients.
Eligibility
Ages Eligible for Study
18 - 79 Years
Genders Eligible for Study
Both
Inclusion Criteria
- Severe carotid artery disease
- Patients who have not had symptoms related to their carotid artery disease in the last 180 days
- Patients who are able to undergo either an interventional stenting or surgical procedure
Exclusion Criteria
- Patients who have had symptoms in the last 180 days
- Patients who are high risk for surgery
- Patients who have certain conditions that might confound the results of the study
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