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临床试验/NCT06045039
NCT06045039招募中不适用

Clinical Efficacy of Stent-balloon-stent (SBS) Technique in the Treatment of Coronary Bifurcation Lesions

Henan Institute of Cardiovascular Epidemiology1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
1
主要终点
Target lesion failure rate

研究概览

简要总结

The treatment of coronary bifurcation lesions continue to remain challenges. Due to the special hemodynamics caused by the special anatomical structure of the coronary bifurcation, it is easy to cause vascular crest displacement and plaque formation. The existing single-stent strategy and double-stent strategy are easy to cause vascular crest offset, stent accumulation, in-stent thrombosis, in-stent restenosis and other poor long-term prognosis. Stent-balloon-stent (Stent-balloon-stent, SBS) technique enables the guide wire to enter the side branch from the mesh at the distal end of the main vascular stent, and the drug balloon is used to dilate the opening of the side branch, so that the opening area of the side branch is more than 5mm².The SBS technique reduces the risk of branch vascular dissection, occlusion, snow shoveling phenomenon, maintain the original state of bifurcated blood vessels to the greatest extent, should have a good impact on the long-term prognosis of patients with coronary bifurcation lesions (CBL). The purpose of this study is to explore the feasibility, safety and effectiveness of SBS technique.

详细描述

This is a study to evaluate the application of stent-balloon-stent (Stent-balloon-stent, SBS) in complex bifurcation lesions. 1-2mm from the side branch (SB) opening, the stent was implanted in the side branch, and then the stent was implanted in the main vessel (MV).The guide wire enters the side branch from the mesh at the distal end of the main vascular stent, and the drug balloon is used to dilate the opening of the side branch, so that the opening area of the side branch is more than 5mm².The patients were examined by coronary angiography before operation and 6-12 months after operation, and the related data such as stenosis rate and minimum lumen diameter of diseased vessels were recorded. The incidence of target vessel failure (TLF) 6-12 months later, including cardiogenic death, target vessel myocardial infarction and clinically driven target vessel revascularization, was taken as the main clinical end point. The corresponding data of the patients before and after operation were obtained, and the clinical efficacy was compared with the existing double stent strategy.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • There is evidence of myocardial ischemia, such as coronary angiography, including patients with stable angina pectoris, unstable angina pectoris, asymptomatic myocardial ischemia and acute myocardial infarction (> 24 hours).
  • All bifurcation lesions were Medina 1, 1, 1 or 0, 1, 1 with reference vessel diameter (RVD) in the SB ≥2.5 mm by visual estimation and had to meet DEFINITION criteria of complex bifurcations
  • Patients who can tolerate long-term antiplatelet therapy
  • None of the vessels related to bifurcation lesions have received stent surgery
  • Patients who agree and sign an informed consent form

排除标准

  • Patients who are unwilling to sign the relevant informed consent form
  • Patients with severe surgical contraindications
  • Life expectancy of patients is less than 12 months
  • Patients who have previously undergone stent implantation or surgical coronary artery bypass grafting for related lesions
  • Patients with severe hepatorenal insufficiency
  • Heart failure patients with NYHA grade ≥ Ⅲ
  • Patients who are scheduled for surgery requiring antiplatelet medication interruption within 6 months
  • Patients who need chronic oral anticoagulation
  • Any clinical condition of the patient may interfere with medication compliance or long-term follow-up
  • Pregnant or breastfeeding women

结局指标

主要结局

Target lesion failure rate

时间窗: 6-12 months

clinically driven target lesion revascularization (TLR)

次要结局

  • minimum lumen area and lumen stenosis rate(6-12months)

研究者

发起方
Henan Institute of Cardiovascular Epidemiology
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xianpei Wang

Chief Physician

Henan Institute of Cardiovascular Epidemiology

研究点 (1)

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