Fondazione Evidence per Attività e Ricerche Cardiovascolari ONLUS
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Late Lumen Loss (LLL) at 6 months follow-up defined as the difference between postprocedural minimum luminal diameter and follow-up minimum luminal diameter, as assessed by quantitative coronary angiography
Device Success: ability of the Investigational Device to be delivered, dilate, and be retrieved from the target lesion.
Procedural Success: defined as Device Success without the occurrence of Major Adverse Cardiac Events (MACE) during the index hospitalization
(and 5 more...)
18 Years and older (Adult, Senior)
March 15, 2010
August 14, 2013
Irccs Fondazione Centro S.Raffaele Del Monte Tabor Milan, MI, Italy
† Study has passed its completion date and status has not been verified in more than two years.