LimbFlow Announces First Patient Treated in U.S. Feasibility Study and Commencement of International Post-Market Study

Physica System Trabecular Titanium Tibial Plate – 1st Surgery Performed by Dr. Ivan De Martino

Luigi Ferrari, LimaCorporate CEO, commented: "TT Tibial plate is an important addition to the Physica system and will enable LimaCorporate to approach a new segment of the total knee market. 

Virtual Short Course Offers New Insights for Corrosion Prevention and Sustainability of Biomedical Implants and Devices

AMPP’s Corrosion Technical Series is now offering a new 6-hour short course on corrosion prevention in metallic biomaterials and biomedical devices.

Dr. Michael Cantor Named Intuition Robotics 1st Chief Medical Officer

The company recently announced its plan to extend to healthcare.

LimFlow SA today announced enrollment of the first patient in the U.S. feasibility study of the LimFlow Percutaneous Deep Vein Arterialization (pDVA) System, a novel, purely percutaneous device for the treatment of end-stage critical limb ischemia (CLI) when all other revascularization efforts have been exhausted.

The first patient was treated on July 5, 2017, at Metro Health – University of Michigan Health by Jihad A. Mustapha, MD, FACC, FSCAI.

LimbFlow reports the feasibility study is a multicenter, prospective, single-arm study to be conducted at three U.S. centers encompassing 10 “no-option” CLI patients. Endpoints include amputation-free survival at one month, patency, limb salvage and wound healing. Subjects will be followed out to two years. This clinical trial is the initial step towards a U.S. approval pathway for the LimFlow System.

“The only other disease with worse life expectancy than CLI is pancreatic cancer. Because of the mortality rate associated with amputations due to ischemia, a new approach to treat CLI is needed now more than ever. In the LimFlow study, we hope to help patients with no other options that are on their way to amputation,” said Dr. Mustapha, the study’s primary investigator.

The Paris-based medical device company also announced the initiation of a multicenter, prospective, single-arm post-market surveillance study, which will enroll up to 50 Rutherford Class 5 and 6 “no-option” patients in several CLI centers of excellence in Europe and Asia. Patients will be followed out to one year, and endpoints include amputation-free survival (AFS) and wound healing progression. Data collection is aligned with the U.S. feasibility study, allowing for a large comparable data set for the use of the LimFlow System in this “no-option” CLI sub-group.

The LimFlow System is designed to restore perfusion to the ischemic foot, which may relieve rest pain, promote chronic wound healing, reduce major amputations and restore mobility for patients when used as part of a multi-disciplinary team approach. It uses proprietary ultrasound-guided catheters and covered nitinol stents to uniquely bypass diseased arteries and divert blood flow into the tibial vein to vascularize the ischemic foot.

Chief Executive Officer Dan Rose concluded, “With approximately 150,000 ischemic amputations annually in the U.S. costing the healthcare system many, many billions of dollars, we look forward to further exploring the promise of LimFlow and its role in treating the epidemic of Critical Limb Ischemia.”

spot_img

DON'T MISS

Subscribe to Medical Device News Magazine here.

Related Articles