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临床试验/NCT04657328
NCT04657328Unknown不适用

Contrast-enhanced Ultrasound in Breast Tumor by Sonazoid

Chinese PLA General Hospital1 个研究点 分布在 1 个国家目标入组 181 人开始时间: 2020年8月15日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
181
试验地点
1
主要终点
Diagnostic performance of contrast-enhanced ultrasound in breast tumor by Sonazoid.

研究概览

简要总结

Sonazoid as a new generation of ultrasound contrast agent.This study based on the features of Sonazoid specific angiography and high mechanical index,the role of Sonazoid in the differential diagnosis of breast benign and malignant tumors was explored.

详细描述

This trial is a prospective, multi-center study.With pathology as the gold standard, based on quantitative and qualitative analysis, Sonazoid-CEUS was compared with MRI to explore the diagnostic efficacy (accuracy, sensitivity and specificity) of Sonazoid-CEUS for breast tumor in different pathological types.

Investigators will also record the parameter information of imaging examination, pathological type of pathological examination and immunohistochemical index.Contrast-enhanced ultrasound includes lesion location, initial peak tumor volume, 1-minute tumor volume, 2-minute tumor volume, and 5-minute tumor volume, as well as the time for contrast enhancement, contrast agent clearance, and contrast agent clearance.Whether there is no enhancement area in the lesion after contrast enhancement, shape after contrast enhancement, edge after contrast enhancement, order of enhancement, uniformity of enhancement, intensity enhancement, pattern of enhancement, clear boundary after contrast enhancement, aspect ratio after contrast enhancement, etc.The magnetic field strength of the equipment is planned to be recorded in the enhanced MRI information, the name of the MRI contrast agent, the lesion location, the size of the LESION, and the scanning performance are enhanced (lump-like enhancement, non-lump-like enhancement, point-like enhancement), time-signal intensity enhancement curve, DWI signal, ADC value, etc.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

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

  • Conventional ultrasonography suggested definite lesions in the breast;
  • In addition to conventional ultrasound, there is also enhanced MRI examination;
  • There are no contraindications for puncture biopsy, and pathological examination (cytology, histology) is planned to examine the patients with target lesions
  • Patients volunteered to participate in the study and signed informed consent.-

排除标准

  • Those who are known to be allergic to ultrasound contrast agents;
  • The subject has a history of allergy to eggs or egg products (i.e. skin rash, dyspnea, swelling of the mouth or throat, hypotension or shock, etc.)
  • Arteriovenous (left and right) shunt patients in the heart and lungs
  • Patients with serious heart disease or serious lung disease
  • Patients who are pregnant, possibly pregnant or lactating
  • Patients who cannot receive contrast agent MRI
  • In addition, the investigator or the patient that the investigator considers not suitable to participate in this study

结局指标

主要结局

Diagnostic performance of contrast-enhanced ultrasound in breast tumor by Sonazoid.

时间窗: 10 months

Pathology as a gold standard,to evaluate the diagnostic performance in breast tumor by Sonazoid.

次要结局

未报告次要终点

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ping Liang

Clinical Professor

Chinese PLA General Hospital

研究点 (1)

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