Study Type
Interventional - Device
The objective of the VELETI II study was to evaluate the efficacy of stenting moderate SVG lesions with paclitaxel-eluting stents and/or PROMUS Element stent on reducing the first occurrence of the composite of cardiac death, myocardial infarction or repeat revascularization related to the target SVG over the duration of follow-up.
Primary Endpoint:
The first occurrence of the composite of cardiac death, myocardial infarction related to the target SVG or coronary revascularization related to the target SVG over the duration of the follow-up.
Jose Rodes-Cabau was the Principal Investigator.
Interventional - Device
Randomized, prospective, multicenter
1
16
125
2011-2016
PHRI
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