Volume 7, Issue 4 , Pages 194-195, December 2004
CaRESS: Carotid Revascularization Using Endarterectomy or Stenting Systems
The primary objective of the CaRESS Phase I trial is to determine the sample size needed to reliably test the hypothesis that carotid stenting systems with distal embolic protection (CAS) is equivalent to carotid endarterectomy (CEA) in the treatment of symptomatic and asymptomatic carotid artery disease in a broad-risk population. A total of 397 patients were treated at 14 clinical centers. The primary endpoint results of combined all-cause mortality and stroke at 30-days and 1-year are presented. The CaRESS Phase I study was able to closely resemble clinical practice and results suggest equivalence between treatment groups.
Keywords: clinical trial , carotid endarterectomy , carotid stenting , stroke
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Affiliations for the members of the CaRESS Steering Committee appear in the acknowledgment section at the end of the article.Funds for the Phase 1 CaRESS Clinical Trial were provided to the International Society of Endovascular Specialists, which sponsored the Investigational Device Exemption, by Boston Scientific Corporation, Natick, MA and Medtronic, AVE, Santa Rosa, CA, USA.
PII: S1089-2516(05)00019-3
doi:10.1053/j.tvir.2005.03.009
© 2005 Elsevier Inc. All rights reserved.
Refers to erratum:
- Erratum
Volume 7, Issue 4 , Pages 194-195, December 2004
