BridgePoint Medical, Inc. has completed the first human clinical case in the United States using its CrossBoss CTO Catheter and Stingray CTO Re-Entry System. The CrossBoss CTO Catheter and Stingray CTO Re-Entry System are under clinical investigation to demonstrate safety and effectiveness in the treatment of completely blocked arteries known as Chronic Total Occlusions (CTO). BridgePoint Medical's clinical trial, Facilitated Antegrade Steering Technique for Chronic Total Occlusions (FAST-CTOs), was conditionally approved in January 2009 by the FDA. The first clinical case was completed by Dr. William Lombardi, Interventional Cardiologist and Cardiac Catheterization Lab Director at North Cascade Cardiology in Bellingham, Washington. The patient was a 61 year old woman with a chronic total occlusion of her right coronary artery, chest pain (characterized as level three angina) and a positive stress test. The patient was referred to Dr. Lombardi for inclusion in BridgePoint Medical's FAST-CTOs clinical trial after a failed treatment attempt to cross the lesion by a referring physician. Procedural completion took 35 minutes, resulting in the opening of the completely blocked vessel and return of normal blood flow to the patient's heart. "The BridgePoint Medical System allowed me to open this challenging total occlusion", stated Dr. Lombardi. "BridgePoint Medical's clinical trial is designed to demonstrate the CrossBoss CTO Catheter and the Stingray Re-Entry System are broadly effective in re-establishing blood flow across completely blocked arteries and these devices will hopefully provide improved options for patient care." The patient was released from the hospital the day after the procedure. "We are very excited about the start of our United States clinical trial" said Chad Kugler, Co-Founder, President and General Manager of BridgePoint Medical. "We believe that our crossing systems will be demonstrated to provide a viable non-surgical alternative to this challenging form of heart disease."