Trial Comparison of Accuseal and Bovine Pericardial Patch During Endarterectomy

Sponsor
CAMC Health System (Other)
Overall Status
Completed
CT.gov ID
NCT01184183
Collaborator
(none)
200
1
28
7.1

Study Details

Study Description

Brief Summary

Carotid Endarterectomy (CEA), surgical removal of the blockage in the neck artery, is the accepted management of choice for significant blockage of the carotid artery. Previous studies showed improved perioperative outcomes and prevention of recurrent blockage by the use of the patch to close the surgical incision in the artery. The ideal patch reduces bleeding and prevents recurrent blockage.This is looking at long-term results toward improvement with the use Accuseal patch than Bovine Patch.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Comparing Accuseal Vs. Bovine Pericardial in CEA

Detailed Description

This study will be a prospective, randomized, evaluation comparing the outcomes resulting from the use of two different patches (Accuseal vs Bovine Pericardial) used for CEA.Our proposed study will evaluate the perioperative (within 30 days of operation) and long-term (6 month, 1 year, 2 year, 3 year) complications associated with the Accuseal and Bovine Pericardial patches. This will include thrombosis of the carotid artery, and the degree of recurrent plaque formation of the patched artery as determined by duplex ultrasound evaluation in the perioperative and long-term periods.Patients will be blinded to the type of patch they received.Survival analysis (Kaplan-Meier) (used in this case for time to the event analysis) will be used for time to restenosis, time to stroke, and time to late death.

Study Design

Study Type:
Observational
Actual Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Randomized Trial Comparison of Accuseal and Bovine Pericardial Patch During Endarterectomy
Actual Study Start Date :
Sep 1, 2009
Actual Primary Completion Date :
Jan 1, 2012
Actual Study Completion Date :
Jan 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Accuseal patch

Procedure: Comparing Accuseal Vs. Bovine Pericardial in CEA
Accuseal patch - The Goretex Company has since designed a new patch, "the Accuseal," which is marketed as decreasing the intra-operative time (i.e, having a short hemostasis time) without affecting the perioperative stroke rate. Bovine Pericardial patch - The Bovine Pericardial patch has been used for nearly two decades, since the late 1990s. However, studies based on retrospective review of data in which patients received the Bovine Pericardial patch, reported the clinical outcomes post-operative stroke, death, time to hemostasis and recurrent restenosis.

Bovine Pericardial patch

Procedure: Comparing Accuseal Vs. Bovine Pericardial in CEA
Accuseal patch - The Goretex Company has since designed a new patch, "the Accuseal," which is marketed as decreasing the intra-operative time (i.e, having a short hemostasis time) without affecting the perioperative stroke rate. Bovine Pericardial patch - The Bovine Pericardial patch has been used for nearly two decades, since the late 1990s. However, studies based on retrospective review of data in which patients received the Bovine Pericardial patch, reported the clinical outcomes post-operative stroke, death, time to hemostasis and recurrent restenosis.

Outcome Measures

Primary Outcome Measures

  1. The aim of this study is to evaluate the perioperative and long-term complications (thrombosis of the carotid artery, and the degree of restenosis of the patched artery as determined by duplex ultrasound evaluation). [within 30 days of operation,6 month, 1 year, 2 year, 3 year]

Secondary Outcome Measures

  1. We hypothesize that the Accuseal patch will have a longer hemostasis time but a lower associated stroke rate and a longer time to restenosis than the Bovine Pericardial patch. [within 30 days of operation,6 month, 1 year, 2 year, 3 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Symptomatic patients with >50% stenosis or Asymptomatic patients >60% stenosis: i.e.: patients experiencing a neurological event(s) such as a trans-ischemic attack, cerebrovascular accident, amaurosis fugax, and/or a preoperative duplex ultrasound, magnetic resonance angiogram, or Angiogram indicative of severe > 60% carotid artery stenosis.
Exclusion Criteria:
  • will be enforced for those less than 18 years of age, patients who for religious reasons can not accept a Bovine Pericardial patch and those with a combined procedure ie: coronary artery bypass graft (CABG) and CEA.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vascular Center of Excellence Charleston West Virginia United States 25304

Sponsors and Collaborators

  • CAMC Health System

Investigators

  • Principal Investigator: Patrick Stone, M.D., Vascular Center of Excellence(CAMC Medical Staff - with admitting privileges)

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Patrick Stone, MD, Patrick Stone, M.D., Vascular Center of Excellence(CAMC Medical Staff - with admitting privileges)., CAMC Health System
ClinicalTrials.gov Identifier:
NCT01184183
Other Study ID Numbers:
  • 09-02-2136
First Posted:
Aug 18, 2010
Last Update Posted:
Feb 19, 2020
Last Verified:
Feb 1, 2020
Keywords provided by Patrick Stone, MD, Patrick Stone, M.D., Vascular Center of Excellence(CAMC Medical Staff - with admitting privileges)., CAMC Health System
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 19, 2020