PLATINUM Long Lesion Trial

Study Objective

Evaluate the safety and effectiveness of the PROMUS Element™ Stent System for the treatment of patients with a de novo lesion > 24 and ≤ 34 mm in length; ≥ 2.50 mm to ≤ 4.25 mm in diameter

Study Design

Prospective, Single-arm, Multicenter

0% ARC ST (Def/Prob) and 0% TV-MI

PLATINUM Long Lesion Trial

2-Year Results2

4.8% TV-MI

SPIRIT PRIME Long Lesion Registry

2-Year Results in Perspective3,4