Healthcare Industry News: Penumbra
News Release - November 1, 2010
Penumbra, Inc. Enrolls First Patients In PULSE Clinical Trial To Evaluate A Fully Retrievable, Dense Mesh Temporary Stent For Immediate Flow Restoration In Interventional Acute Ischemic Stroke TreatmentALAMEDA, Calif.--(Healthcare Sales & Marketing Network)-- The Stroke Teams at the University Hospital Dresden in Dresden, Germany, and the University Hospital Göttingen in Göttingen, Germany, have enrolled the first patients in an international clinical trial to assess the safety and effectiveness of aspiration with the Penumbra System® in conjunction with the Pulse™ flow restoration device. Following on the demonstrated safety and marked effectiveness of the Penumbra System, the PULSE trial aims to demonstrate the performance of an additional adjunctive mode of immediate flow restoration using a temporary stent.
“A quick and complete reperfusion of brain tissue is important in the acute phase of many strokes in which a major brain artery is blocked. Mechanical devices designed for intra-arterial use may prove to be more effective than IV thrombolysis in achieving that goal,” said Prof. Dr. Michael Knauth, Director, Department of Neuroradiology, University of Göttingen.
The Pulse flow restoration device is a self-expanding, fully retrievable, dense mesh temporary stent designed to be deployed into a clot blocking blood flow to the brain. The Pulse flow restoration device is designed to offer immediate flow restoration while simultaneously allowing the continued aspiration of clot using the Penumbra System. It was designed by Penumbra’s research and development team, which has over twelve years of industry experience focused on the application of nitinol stent technology for the treatment of neurovascular diseases including aneurysms, intracranial stenosis, and acute stroke.
The Penumbra System continuous aspiration thrombectomy devices are used by neuro interventional specialists to gently remove clots from the large vessels of the brain that are causing an acute stroke. The Penumbra System has been commercially available worldwide for three years and is now used in the majority of patients interventionally treated for acute ischemic stroke.
Penumbra, Inc. is an independent medical device company employing over 300 people worldwide and committed to delivering clinically beneficial products that help patients suffering from stroke and other neurovascular diseases. Penumbra’s global headquarters is located in Alameda, California with sales operations in North and South America, Europe, Australia and Asia.
Issuer of this News Release is solely responsible for its
Please address inquiries directly to the issuing company.