跳至主要内容
临床试验/NL-OMON42877
NL-OMON42877已完成不适用

Feasibility of contrast enhanced ultrafast ultrasound to determine aortoiliac blood flow - echoPIV study

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 15 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • healthy, slim (BMI below 22), willingness to undergo MRI scan, willingness to undergo echoPIV examination

排除标准

  • * Hypersensitivity to the active substance(s) or any of the excipients in SonoVue
  • * Right-to-left cardiac shunt
  • * Severe pulmonary hypertension (pulmonary artery pressure > 90mmHg)
  • * Uncontrolled systemic hypertension
  • * Pregnancy
  • * Lactation
  • * Participation in another clinical trial within 3 months prior to the experimental day
  • * The standard MRI exclusion criteria (pacemakers, cerebral vascular clips, pregnancy, claustrophobia)

研究者

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