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Prospective,Multicenter Study of Randomized Comparison of the Biolimus A9-eluting Stent With the Zotarolimus-eluting Stent in Multi-vessel PCI
The risk of restenosis in the treatment of coronary artery disease has significantly lessened thanks to the introduction of Drug eluting stent. Yet, debates on the efficacy and safety of stents in complex lesions or patients have been circulated. Recently, PCI in multiple lesions is universally performed with the development of effective stents in various kinds in the clinics. However, a randomized study is rare for multi-vessel coronary artery disease in real procedural environments. The primary purpose of this study is to evaluate the clinical progress of biolimus A9-eluting stent and zotarolimus-eluting stent in multi-vessel coronary artery disease.
The patients who need multi-vessel stenting with multi-vessel coronary artery disease will be enrolled.Each randomization of the enrolled subjects will be done 1:1 (biolimus A9-eluting stent : zotarolimus-eluting stent). Randomization will be stratified by two factors: Diabetes mellitus and Acute coronary syndrome.Clinical follow-up will occur at the following time points; 1 month, 1 year and 2 years.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Chonnam National University Hospital
Kwangju, Chonnam, South Korea
Ulsan University Hospital
Ulsan, Gyeongsangbuk-do, South Korea
Inje University Ilsan Paik Hospital
Ilsan, Kyeongki, South Korea
Kosin University Hospital
Busan, South Korea
Daegu Catholic University Medical Center
Daegu, South Korea
Daegu Fatima Hospital
Daegu, South Korea
KyungPook National University Hospital
Daegu, South Korea
Yeungnam University Hospital
Daegu, South Korea
Seoul National University Hospital
Seoul, South Korea
Start Date
March 1, 2013
Primary Completion Date
June 1, 2021
Completion Date
June 1, 2021
Last Updated
September 1, 2021
932
ACTUAL participants
Percutaneous Coronary Intervention
PROCEDURE
Lead Sponsor
Keimyung University Dongsan Medical Center
NCT01311323
NCT07133984
Data Source & Attribution
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