Crux Biomedical’s Vena Cava Filter Presented at Society Of Interventional Radiology Meeting: 98% Success Rate Shown in Trial to Prevent Recurrent Pulmonary Embolism
Published: Mar 26, 2012
By obstructing the blood flow through the lungs, PE cause difficulty breathing, chest pain and palpitations. Each year in the United States, approximately 600,000 patients develop PE and an estimated 200,000 deaths occur.
The primary means of prevention and therapy of PE is systemic administration of anticoagulant agents, but is contraindicated in many patients. These patients require alternate treatments to reduce the ongoing PE risk, including vena cava filters – small devices that are inserted in the inferior vena cava, the main blood vessel returning blood from the lower part of the body to the heart, to prevent blood clots from reaching the lungs.
The Crux Biomedical VCF was designed to address the limitations of currently available VCFs, including perforation, migration and inability to retrieve. "Crux designed a device that is both more versatile and simple to use," stated Tom Fogarty, M.D., noted cardiovascular surgeon and founder of Crux Biomedical.
“The Crux device demonstrated an excellent safety profile,” stated Robert R. Mendes, M.D., Principal Investigator of the study; Associate Professor of Surgery, University of North Carolina; and Chief of Vascular Surgery, Rex UNC Healthcare. “The clinical study evaluation has demonstrated the Crux VCF System device can be used safely for the prevention of recurrent PE.”
The recently completed pivotal trial, known as the RETRIEVE Clinical Study, was a prospective, single-arm, multinational investigational study to assess the safety, performance, and efficacy of the Crux VCF System as both a retrievable and a permanent device. The trial included 125 patients at high risk for PE and was performed at 22 centers in the United States, Australia, New Zealand and Belgium.
In the study, the technical success rate of filter deployment was 98 percent; filter retrieval success was also 98 percent. The average retrieval time was 7 minutes, with the femoral approach used for retrieval in 70% of cases. By the 6-month follow up of the study (CONFIRM), no embolizations, migrations, or fractures were observed.
The presentation at the SIR 2012 Annual Scientific Meeting, titled “The Results of the Crux Vena Cava Filter RETRIEVE Trial” was authored by Robert R. Mendes, M.D., and was presented on Sunday, March 25 at 11:50 am Pacific Time during the IVC Filters Scientific Session in the Moscone Center, Room 122.
The Crux VCF has received CE Mark approval for commercial use in the European Union. The System is being studied in the United States under an approved Investigational Device Exemption (IDE) Study. 510(k) Clearance for commercial distribution in the U.S. is pending.
Crux Biomedical is located in Menlo Park, California and is focused on developing improved therapies for the human vasculature. It is funded by Alloy Ventures, Three Arch Partners, Emergent Medical Partners and Thomas Fogarty, M.D. Additional information is available at www.cruxbiomedical.com.
For Crux Biomedical
Ed Stevens, 727-327-3396