Newswise — PinnacleHealth CardioVascular Institute enrolled the first patient in Pennsylvania into the TOBA II clinical on October 19, 2015. This trial is to assess the safety and efficacy of a vascular implant for the treatment of dissections (tearing in the artery wall) that occur following balloon angioplasty (PTA) of the main artery in the leg.
The TOBA II study is designed to enroll 210 subjects at up to 40 sites in the United States and Europe. William Bachinsky, MD, FACC, medical director of vascular services at PinnacleHealth CardioVascular Institute, serves as principal investigator locally at PinnacleHealth.
The first Pennsylvania patient is from the Harrisburg area and was unable to walk more than a short distance before the procedure without feeling symptoms. All study subjects in TOBA II suffer from advanced peripheral artery disease in one or both legs. They are treated with the Tack Endovascular System™ following standard balloon angioplasty or drug-coated balloon angioplasty in the superficial femoral and proximal popliteal arteries when a dissection occurs (see www.TOBA-II.com for details).
The Tack™ implant supports the specific area of dissection and allows the vessel to heal, while preserving the areas that are open and don’t require additional treatment such as stenting. This “Tacking” approach minimizes the metal left in the artery and the vessel inflammation that can result from traditional stenting.
“We are very excited about having this cutting edge technology available at PinnacleHealth for patients with claudication—or pain in the legs—due to leg artery blockages,” said Dr. Bachinsky. “The Tack implant could be a ‘game changer’ by reducing the re-narrowing that can be seen following PTA, allowing for greater flexibility within the artery, and potentially reducing the risk for implant fracture.”
For more information, contact Gretchen Meise, RN, at (717) 920-4400 x4280 (office), or [email protected].
Tack Endovascular System™ and Tack™ are trademarks of Intact Vascular, Inc."CAUTION: Investigational device. Limited by Federal (United States) law to investigational use."The Tack Endovascular System is “Not Approved for Sale in the United States.” The Tack Endovascular System is CE Mark authorized under EC Directive 93/42/EEC.
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