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临床试验/NCT02652689
NCT02652689终止不适用

Transthoracic Parametric Doppler Assessment of Lung Doppler Signals in Acute Pulmonary Embolism

Echosense Ltd.1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2016年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
25
试验地点
1
主要终点
Identify lack of Lung Doppler signals in specific lung sections that were diagnosed obstructed by CT

研究概览

简要总结

The LDS may contain information of significant diagnostic and physiological value regarding the pulmonary parenchyma and vasculature, as well as the cardio- vascular system in general. In pilot clinical studies of patients with acute decompensated heart failure (ADHF) as well as patients with Pulmonary Hypertension, LDS signals patterns unique to these conditions were identified. We believe that these newly discovered ultrasound signals might provide a non-invasive radiation-free means to diagnose and monitor patients with Pulmonary Embolism.

The purpose of this study is to assess the utility of noninvasive assessment of lung Doppler signals performed via transthoracic parametric Doppler. The objective of the study is to evaluate the lung Doppler signals (LDS) in patients diagnosed with acute PE, in order to determine the potential assessment value of this non-invasive method in this potentially life threatening condition.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
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

  • Confirmed diagnosis of acute PE on CTA

排除标准

  • Pregnant women
  • Inability to consent
  • Patients with severe chest wall deformity
  • Previously diagnosed PE
  • Pneumonia
  • Pulmonary edema
  • Pneumothorax
  • Severe COPD (gold class III, IV)
  • Hemodynamically unstable patients

研究组 & 干预措施

Diagnostic ultrasound

Experimental

Recording Doppler ultrasound signals noninvasively from the right chest wall

干预措施: Diagnostic ultrasound radiation (Radiation)

结局指标

主要结局

Identify lack of Lung Doppler signals in specific lung sections that were diagnosed obstructed by CT

时间窗: 30min

The obstructed sections will be compared with healthy lung sections

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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