scholarly journals TCTAP A-025 Efficacy of Long 2nd Generation Drug-Eluting Stent Implantation from Healthy to Healthy Segment Under Intravascular Ultrasound Guidance in Acute Myocardial Infarction

2016 ◽  
Vol 67 (16) ◽  
pp. S10-S11
Author(s):  
Shota Ikeda ◽  
Takahiro Watanabe ◽  
Yuichi Hanaki ◽  
Tomoyuki Fukuzawa ◽  
Shingo Tanaka ◽  
...  
2008 ◽  
Vol 51 (3) ◽  
pp. 189-195 ◽  
Author(s):  
Hajime Fujimoto ◽  
Susumu Tao ◽  
Jun Masuda ◽  
Haruo Mitani ◽  
Sachiko Ito ◽  
...  

BMJ Open ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. e052215
Author(s):  
Pil Hyung Lee ◽  
Soon Jun Hong ◽  
Hyun-Sook Kim ◽  
Young won Yoon ◽  
Jong-Young Lee ◽  
...  

IntroductionAngiography remains the gold standard for guiding percutaneous coronary intervention (PCI). However, it is prone to suboptimal stent results due to the visual estimation of coronary measurements. Although the benefit of intravascular ultrasound (IVUS)-guided PCI is becoming increasingly recognised, IVUS is not affordable for many catheterisation laboratories. Thus, a more practical and standardised angiography-based approach is necessary to support stent implantation.Methods and analysisThe Quantitative Coronary Angiography versus Intravascular Ultrasound Guidance for Drug-Eluting Stent Implantation trial is a randomised, investigator-initiated, multicentre, open-label, non-inferiority trial comparing the quantitative coronary angiography (QCA)-guided PCI strategy with IVUS-guided PCI in all-comer patients with significant coronary artery disease. A novel, standardised, QCA-based PCI protocol for the QCA-guided group will be provided to all participating operators, while the PCI optimisation criteria will be predefined for both strategies. A total of 1528 patients will be randomised to either group at a 1:1 ratio. The primary endpoint is the 12-month cumulative incidence of target-lesion failure defined as a composite of cardiac death, target-vessel myocardial infarction or ischaemia-driven target-lesion revascularisation. Clinical follow-up assessments are scheduled at 1, 6 and 12 months for all patients enrolled in the study.Ethics and disseminationEthics approval for this study was granted by the Institutional Review Board of Asan Medical Center (no. 2017-0060). Informed consent will be obtained from every participant. The study findings will be published in peer-reviewed journal articles and disseminated through public forums and academic conference presentations. Cost-effectiveness and secondary imaging analyses will be shared in secondary papers.Trial registration numberNCT02978456.


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