Coronary Artery Disease Clinical Trial
Official title:
A Prospective Three-arm Multi-center Study to Investigate Procedural, Clinical and Angiographic Outcomes Using a Drug Eluting Balloon Versus a Standard Balloon in Combination With a Bare Metal Stent and a DES Stent, Following the Provisional Side Branch T-stenting Approach, in Patients With Complex Lesions
The purpose of the DEBIUT study is to assess procedural, clinical and angiographic outcomes
of:
1. Provisional T-stenting use for dilation the Paclitaxel-eluting PCI-balloon (DiorTM) in
comparison to dilation with a standard balloon prior to the implant of the Liberty Bare
Metal Stent in bifurcation lesions (with side branch involvement).
2. Comparison of the results above with the results of using a standard balloon prior to
provisional T-stenting with the Paclitaxel-eluting stent TaxusTM LibertéTM.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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