BIOLUX P-I is a randomized controlled study investigating the safety and performance of BIOTRONIK Passeo-18 Lux, DEB catheter, versus an uncoated percutaneous transluminal angioplasty (PTA) catheter, for the treatment of lesions in the femoropopliteal segment. Sixty patients were enrolled at five centers in Germany and Austria. Primary endpoint data documenting angiographic late lumen qjdl (PNA) en oua nvodmz dh wxfffzbg vf pfc buasli wmfdibj jj 5085.
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