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Clinical Trial Summary

Multi-center, dual cohort (randomized and single vessel) study designed to demonstrate feasibility, initial safety and performance of the Kips Bay Medical, Inc. eSVS® Mesh as an external vein support device for use over saphenous vein grafts during coronary artery bypass surgery. In the Randomized Cohort, each study subject will receive a SVG without Mesh (control) and a SVG with the eSVS Mesh (treatment). In the Single Vessel Cohort, each study subject will receive one SVG with the eSVS Mesh.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Atherosclerosis
  • Atherosclerosis of Autologous Vein Coronary Artery Bypass Graft(s)

NCT number NCT01676376
Study type Interventional
Source Kips Bay Medical, Inc.
Contact Rebecca Wetterling
Phone 763-235-3540
Email clinical@kipsbaymedical.com
Status Recruiting
Phase Phase 1/Phase 2
Start date August 2012
Completion date June 2020