CorMatrix ECM for Carotid Repair Following Endarterectomy Registry

Completed

Conditions studied: Carotid Stenosis

In brief

Assess device performance data from subjects undergoing patch angioplasty of the carotid artery following carotid endarterectomy using the CorMatrix ECM for Carotid Repair.

Key facts

Study ID

NCT01569594

Run by

Elutia Inc.

People needed

230

Starts

2012-04-01

Expected to finish

2016-12-31

Last updated by the study team

2023-07-21

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must be undergoing carotid endarterectomy with patch angioplasty closure.
• Subject's operative surgeon intends to use CorMatrix ECM as the patch material for closure of the carotid artery per its FDA cleared Indications for Use.
• The subject must possess the ability to provide written Informed Consent.
• The subject must express an understanding and willingness to fulfill all of the expected requirements of this clinical protocol.

You may not qualify if…

• Subjects with a known sensitivity to porcine material.

Where it is running

• Cardio-Thoracic Surgeons, P.C. Trinity — Birmingham, Alabama, United States
• Vascular Surgical Associates P.C. — Marietta, Georgia, United States
• Cardiac Surgery Associates — Indianapolis, Indiana, United States
• St Luke's Hospital — Kansas City, Missouri, United States
• Cardiovascular Surgery Clinic, PLLC — Memphis, Tennessee, United States
• UVA Heart and Vascular Center — Charlottesville, Virginia, United States

Full record on ClinicalTrials.gov

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