Drug Eluting Balloon
DevicePCI using paclitaxel-eluting SeQuent® Please balloon, B. Braun Melsungen AG, Berlin, Germany
NCT Number: NCT01574534
The investigators hypothesize that in a real-world population undergoing percutaneous coronary intervention (PCI) for de-novo stenoses in small native vessels with a diameter <3 mm, drug eluting balloons (DEB) are non inferior to third-generation drug eluting stents (DES).
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Medizinische Universität Graz Kardiologie, Graz, Austria
Drug-eluting balloons are an established treatment for in-stent stenoses and showed good results in small vessels. Moreover, the available data suggest that DEB are a promising new technique for the treatment of de-novo stenoses in small vessels if pre-dilatation is performed and geographical mismatch is avoided.
The aim of this study is to demonstrate that DEB is non-inferior to DES in a real-world population with respect to the combined clinical endpoint Major adverse cardiac events (MACE), defined as cardiac death, non-fatal myocardial infarction, and target vessel revascularization after 12 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PCI using paclitaxel-eluting SeQuent® Please balloon, B. Braun Melsungen AG, Berlin, Germany
PCI using paclitaxel-eluting Taxus Element® stent, Boston Scientific Corp, Natick MA
Time frame: 12 month
Major adverse cardiac events (MACE), defined as cardiac death, non-fatal myocardial infarction, and target vessel revascularization after 12 months.
Time frame: 24/36 month
MACE after 24 and 36 months
Time frame: 12/24/36 month
The single components of the primary endpoint including target lesion revascularization after 12, 24, and 36 months
Time frame: 12/24/36 month
Possible, probable, and definite stent thrombosis defined according to the ARC criteria after 12, 24, and 36 months; all stent thromboses defined according to the ARC criteria after 12, 24, and 36 months
Time frame: 12/24/36 month
Thrombolysis In Myocardial Infarction (TIMI) major bleeding after 12, 24, and 36 months
Net clinical benefit consisting of the primary endpoint and the TIMI major bleeding after 12, 24, and 36 months
Time frame: 12/24/36 month
Cost-effectiveness of DEB vs. DES after 12, 24, and 36 months
Time frame: 12 months
QCA of patients who had events which required CAG/PCI after Baseline PCI
Time frame: 12 months
Outcome analyis of patients with high bleeding risk with regard to Major bleeding events (BARC)
Time frame: 12 months
Difference of the Population with acute versus stable CAD with regard to baseline characteristics, primary and secondary outcome measures (MACE, stent thrombosis, major bleeding)
Time frame: 12 months
Difference of the diabetic versus non-diabetic population regarding baseline characteristics and primary and secondary outcome measures (MACE, stent thrombosis, major bleeding)
Time frame: 12 months
sex specific difference in baseline charchteristics, Impact of sex on safety and efficacy in the stent-free strategy regarding primary and secondary endpoint (MACE, stent thrombosis, major bleeding)
University Hospital, Basel, Switzerland
Other
A Prospective, Randomized, Controlled, Open Label, Multicenter Trial to Test the Non-inferiority of Drug Eluting Balloon vs. Drug Eluting Stent Treatment in de Novo Stenoses of Small Native Vessels Regarding Efficacy and Safety
Acronym: BASKET-SMALL2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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