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临床试验/NCT05410678
NCT05410678已完成4 期

Safety And Efficacy Results of Percutaneous Renal Stent Implantation in Patients With Acute Coronary Syndrome With Ectatic and Aneurysmatic Coronary Arteries

Bursa Postgraduate Hospital0 个研究点目标入组 63 人开始时间: 2015年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
63
主要终点
primary endpoints

研究概览

简要总结

The aim of this study was to evaluate the efficacy and safety of renal stents implanted in ectatic/aneurysmatic coronary arteries.

详细描述

In total, 18 patients (renal stent group) who underwent renal stent implantation in ectatic/aneurysmatic coronary arteries requiring percutaneous coronary intervention (PCI) and 45 patients who underwent large-sized bare metal coronary stent (BMCS) implantation (BMCS group) at our centre between 2015 and 2020 were included in the study. Control coronary angiography (CAG) was performed during the follow-up of these patients, and angiography-guided quantitative measurements were performed during PCI. The primary endpoints were myocardial infarction and cardiovascular mortality, and the secondary endpoints were restenosis and all-cause mortality.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Acute coronary syndrome patients
  • 18 year age
  • ectatic/aneurysmatic coronary arteries

排除标准

  • Patients who underwent elective procedures,
  • experienced unsuccessful attempts
  • referred to surgical revascularization

研究组 & 干预措施

renal stent group

Experimental

Acute coronary patients treatment with renal stent

干预措施: Renal stent (Drug)

BMCS group

Active Comparator

Acute coronary patients treatment with bare-metal stent

干预措施: Renal stent (Drug)

结局指标

主要结局

primary endpoints

时间窗: 2 year

Rate of myocardial infarction and cardiovascular mortality

次要结局

  • secondary endpoints(2 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hasan ARI

Prof. Dr.

Bursa Postgraduate Hospital

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