TINTIN is a physician initiated, prospective, single arm multicenter, Belgian trial, that investigates the safety and efficacy of the treatment with luminor DCB and iVolution self-expanding stent in TASC C and D femoropopliteal lesions of 240mm average.

The 1-year clinical outcomes of TINTIN Trial were presented at LINC 2020 by Dr Koen Deloose (Dendermonde, Belgium) who stated, during his presentation, that: “The combination of luminor DCB and iVolution self-expanding stent, shows impressive 1-year outcomes in the TINTIN trial, comparable to DEs but in more complex lesions”.

TINTIN 1-year outcomes show a Primary Patency of 90.5%, freedom from TLR of 94.4%. Safety has been proved with 0 device related deaths.

>> Official article @ iVascular.global

>> T.I.N.T.I.N. trial : Final 12-month data with the combination of Luminor DCB + iVolution stent in TASC C and D lesions