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INPACT AV Drug-Coated Balloon Is First And Only To Show Superior And Sustained Results Through Two Years Compared To PTA In Treating Arteriovenous Fistulae Lesions
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IN.PACT AV Access Trial 24 Month Results Presented as a Podium First at Charing Cross Symposium
DUBLIN and LONDON, April 20, 2021 /PRNewswire/ Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced the safety and effectiveness results through 24 months for the IN.PACT AV Access clinical study. The data, which were presented virtually as a podium first at the 2021 Charing Cross Symposium, demonstrated that the IN.PACT™ AV drug-coated balloon (DCB) is the first and only DCB to show sustained and superior effectiveness through two years compared to standard percutaneous transluminal angioplasty (PTA) in end-stage renal disease (ESRD) patients with de novo or non-stented restenotic native arteriovenous fistulae (AVF) in the upper extremity.