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CORE 320 Set to Validate Dynamic Volume CT

Article-05a-2009-01

As the next phase in validating advanced computed tomography technology in a clinical setting, Toshiba Medical Systems Corporation (TMSC) is supporting CORE 320, the largest worldwide multi-center trial comparing the effectiveness of 320-detector row dynamic volume CT to SPECT technology. The trial is examining whether the combination of CT angiography and myocardial perfusion can identify coronary stenoses that are less than or equal to 50 percent by Quantitative Coronary Analysis (QCA) and correspond to a SPECT perfusion defect.

“One of Toshiba’s core missions is to validate its technology through clinical trials by leaders in the medical field,” explained Yusuke Toki, general manager, Clinical Application Research Center, TMSC. “As the first and largest multi-center trial using dynamic volume CT, CORE 320 will result in the most statistically reliable data available on this advanced technology. This will be attributed in part to the trial’s design, which calls for an international, multi-center approach, bypassing the limitations associated with focusing on one geographic area and/or small patient populations.”

CORE 320′s multi-center trial will be lead by primary investigator Dr. João A. C. Lima of Johns Hopkins University School of Medicine, in Baltimore, Md. Johns Hopkins University will also serve as the core site for CT. Dr. Marcelo Di Carli of Brigham and Women’s Hospital, a Harvard teaching hospital, in Boston, Mass. will serve as core site for SPECT. Additional investigation sites will be announced in the coming months.

“We expect CORE 320 findings to impact the way the medical community views the role of dynamic volume CT in the diagnosis and treatment of life-threatening diseases,” explained Toki. “These results eventually could impact they way patients are diagnosed and treated.”

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Category: Medical Equipment

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