跳至主要内容
临床试验/NCT03055780
NCT03055780已完成不适用

Clinical Trial for SURECardio CT-FFR

Toshiba Medical Systems Corporation, Japan0 个研究点目标入组 59 人开始时间: 2015年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
59
主要终点
Sensitivity and specificity of SURECardio CT-FFR to detect functionally significant coronary stenosis

研究概览

简要总结

The aim of this study was to determine the diagnostic accuracy of SURECardio CT-FFR to detect functionally significant coronary stenosis.

详细描述

CT acquision and invasive FFR measurement is performed for each patients. The diagnostic accuracy of coronary CTA and SURECardio CT-FFR is investigated using Invasive FFR is used as the reference standard.

研究设计

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

入排标准

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

入选标准

  • suspected coronary artery disease
  • hemodynamically stable condition

排除标准

  • hemodynamic instability
  • atrial fibrillation
  • morbid obesity (BMI≥40 kg/m2)
  • previous stent implantation
  • recent myocardial infarction (within 30 days)
  • age <40 years
  • renal insufficiency (eGFR <60mL/min/1.73m2)
  • bronchospastic lung disease requiring long term steroid therapy

结局指标

主要结局

Sensitivity and specificity of SURECardio CT-FFR to detect functionally significant coronary stenosis

时间窗: one day

次要结局

未报告次要终点

研究者

发起方
Toshiba Medical Systems Corporation, Japan
申办方类型
Industry
责任方
Sponsor

相似试验