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临床试验/NL-OMON47765
NL-OMON47765已完成不适用

18F-Flutemetamol PET/MRI for detection of plaque vulnerability in atherosclerosis - PET/MRI and plaque vulnerability: Flutemetamol

Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 25 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
发起方
入组人数
25

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

  • Age 18 years and older (no maximum age)
  • Informed consent by signed informed consent form regarding this study
  • Either: Patients, who are scheduled for carotid endarterectomy (CEA)
  • Or: Patients who are not scheduled to undergo a CEA, but have experienced a
  • TIA/CVA/amaurosis fugax within the last 14 days and at least a 30% stenosis of
  • the symptomatic carotid artery as based on imaging.

排除标准

  • Severe cognitive impairment, neurological deficit or comorbidity causing the
  • study to be too high a burden for the patient or disrupting patient*s
  • co-operation with scan procedures.
  • Evident other causality for stroke (cardiac embolus, small vessel disease,
  • carotid dissection or thrombogenic diathesis).
  • Pregnant women and nursing mothers.
  • Contra-indications for MRI.
  • *Relative contra-indications for MRI-contrast agent: GFR
  • <30ml/min/1,73m2/Previous allergic reaction to MRI contrast agent.
  • Contra-indication Flutemetamol: Hypersensitivity to the active substance or to
  • any of the excipients, severe liver dysfunction

研究者

发起方
Medisch Universitair Ziekenhuis Maastricht

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