News | December 21, 2010

U.S. Centers Begin CoreValve Clinical Trial Implants

December 22, 2010 – The first implants of the Medtronic CoreValve transcatheter aortic valve were made this week in the pivotal U.S. clinical trial.

The first CoreValve transcatheter aortic valve implantation (TAVI) procedure was performed by David H. Adams, M.D., and Samin K. Sharma, M.D., at The Mount Sinai Medical Center in New York City. A second CoreValve case took place this week at El Camino Hospital in Mountain View, Calif.; St. Francis Hospital, The Heart Center in Roslyn, N.Y., also has been activated in the trial and is screening patients.

CoreValve is a new treatment alternative to open?heart surgery for patients with severe aortic stenosis. It will be investigated in more than 1,200 patients at up to 40 U.S. clinical trial sites.

“Through this trial, we are investigating a minimally invasive, nonsurgical alternative to open?heart surgery for valve replacement in patients with severe aortic stenosis,” said Adams, who is chair of the department of cardiothoracic surgery at Mount Sinai and is a national co?principal investigator of the CoreValve U.S. clinical trial. “This study will evaluate the safety and efficacy of the CoreValve system for use in the United States, where many thousands of patients are diagnosed with severe aortic stenosis every year.”

The CoreValve System is designed with self?expandable technology to replace a diseased aortic valve percutaneously, usually through the femoral artery, without open?heart surgery or surgical removal of the native valve. The CoreValve device is delivered through a controlled deployment delivery system.

“We are very excited with this first step in bringing this important transformational therapy to patients in the United States with life?threatening aortic valve disease, particularly those patients who have limited surgical options,” said Jeffrey Popma, M.D., national co?principal investigator of the CoreValve U.S. pivotal trial and director, interventional cardiology at the Beth Israel Deaconess Medical Center in Boston.

The CoreValve System with the AccuTrak stability layer will be investigated in two independent studies, evaluating patients who have been deemed at high risk for aortic valve surgery and those who have been deemed at extreme risk for aortic valve surgery (i.e., inoperable). Clinical sites across the U.S. will be identified on www.clinicaltrials.gov.

For more information: www.aorticstenosistrial.com

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