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CorMatrix ECM for Carotid Repair Following Endarterectomy Registry

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
CorMatrix Cardiovascular, Inc.
ClinicalTrials.gov Identifier:
NCT01569594
First received: March 30, 2012
Last updated: July 25, 2012
Last verified: July 2012
History of Changes
  Purpose

The objective of this registry is to capture and assess device performance data from subjects undergoing patch angioplasty of the carotid artery following carotid endarterectomy using the CorMatrix ECM for Carotid Repair per its FDA cleared Indications for Use. This registry provides an ongoing post-market surveillance mechanism to document clinical outcomes on the use of the CorMatrix ECM for Carotid Repair.


Condition Intervention
Carotid Stenosis
 Device: CorMatrix ECM for Carotid Repair

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: CorMatrix® ECM® for Carotid Repair Following Endarterectomy Registry

Resource links provided by NLM:

MedlinePlus related topics: Angioplasty
U.S. FDA Resources

Further study details as provided by CorMatrix Cardiovascular, Inc.:

Primary Outcome Measures:
  • Carotid procedure and device related adverse events to determine device performance [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    Carotid procedure and device related adverse events to determine device performance


Estimated Enrollment: 230
Study Start Date: April 2012
Groups/Cohorts Assigned Interventions
Carotid Endarterectomy Subjects Device: CorMatrix ECM for Carotid Repair
Subjects must be undergoing carotid endarterectomy with patch angioplasty closure

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Up to 230 subjects may be enrolled from up to ten U.S. clinical sites

Criteria

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • Subjects with a known sensitivity to porcine material.
  Contacts and Locations
No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: CorMatrix Cardiovascular, Inc.
ClinicalTrials.gov Identifier: NCT01569594     History of Changes
Other Study ID Numbers: 11-PR-1021
Study First Received: March 30, 2012
Last Updated: July 25, 2012
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Carotid Stenosis
Carotid Artery Diseases
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
 Nervous System Diseases
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on May 16, 2013