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临床试验/NL-OMON52121
NL-OMON52121招募中不适用

High-frame-rate contrast-enhanced echocardiography for left-ventricular perfusion analysis after PCI (QUANTO) - High-frame-rate contrast echocardiography

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 65 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
65

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 99(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • Aged >= 18 years.
  • Capable of understanding and signing informed consent.
  • o scheduled for conventional contrast-enhanced echocardiography
  • o Admitted to the Erasmus MC Cardiology ward for an elective cardiac procedure
  • o Admitted to the Erasmus MC Cardiology ward
  • o Planned for cardiac surgery
  • Stage 4A:
  • o underwent PCI in the past hour;
  • o is recovering in the medium-care unit;
  • o is physiologically stable and awake;
  • o suffered a single-vessel ST-elevated myocardial infarction
  • o still carries an intravenous line;
  • o oral explicit approval by the treating intervention cardiologist to perform a
  • contrast-enhanced echographic study in the medium-care unit for this patient.
  • Stage 4B:
  • o Was included in stage 4A, at most 6 months before (range: 3 - 6 months)
  • o Is physiologically stable
  • o Has had no serious adverse events or other cardiac complaints/STEMIs in the

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • Patients living abroad or who are not Dutch speaking;
  • Any contra-indication for contrast media Sonovue (Bracco International bv,
  • Amsterdam), or Luminity (Dutch supplier: LamePro bv, Breda);
  • Patients with inability to obtain adequate echocardiographic examination;
  • Pregnant and/or lactating women

研究者

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