Thirty patients successfully treated with no device-related adverse events using PICSO®

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The study enrolment was completed in several European centres of excellence with Prof. Jan Piek at the Academic Medical Center in Amsterdam as the Principal Investigator.

 

“We are extremely pleased by this milestone achievement for our breakthrough PICSO® System. Preclinical and clinical evidence suggest that PICSO provides significant benefits for patients, reducing not only their ST-segment elevation, but also tissue bleeding and infarct size. We now intend to expand the use of PICSO to additional centres throughout Germany and the UK to provide more patients access to this new therapy with CE-marked PICSO®,” said Ludwig Gold, COO & CFO of Miracor.

 

The Miracor PICSO® Impulse System is designed to treat acute heart attack STEMI patients to complement coronary angioplasty. ‘STEMI’ is an acronym meaning ST-segment Elevation Myocardial Infarction. Heart attacks are divided into three types, according to their severity. A STEMI heart attack is the most severe type. In a STEMI heart attack, the coronary artery is completely blocked off by the blood clot, and as a result virtually all the heart muscle being supplied by the affected artery starts to become necrotic.

 

“We continue to expect that PICSO® will evolve into a standard of care that complements primary PCI procedures,” added Roger Kessels, PhD, Clinical Director at Miracor. “The fact is that despite a promising coronary angioplasty, impaired microcirculation still materialises in nearly one in three STEMI patients, and this frustrating incidence is directly connected to undesired outcomes for patients,” said Dr. Kessels.