跳至主要内容
临床试验/NCT05122416
NCT05122416终止不适用

Optimization of Spleen VCTE Examinations with FibroScan

Echosens4 个研究点 分布在 3 个国家目标入组 433 人开始时间: 2022年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Echosens
入组人数
433
试验地点
4
主要终点
Success rate of the spleen stiffness measurement (SSM) exam with both the optimized M+ probe and the exploratory XL+ probe, defined with at least 8 valid measurements after the exam quality control

研究概览

简要总结

This is an European, prospective, interventional, and multicenter clinical investigation which main objective is to develop a spleen examination dedicated to overweight or obese patients and assess its applicability. It will take place in 4 sites (1 site in the Netherlands, 2 sites in Spain and 1 site in Romania) to include a total of 500 patients (adults and children).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Adult or pediatric patient able to give written informed consent (parents/legal tutors in case of minor patients),
  • Patient affiliated to the healthcare system
  • Adult or children patient followed for a liver disease a suspicion of liver disease or for a consequence of a liver disease, with or without splenomegaly and having a spleen to skin distance (SSD) measurement performed during the screening ultrasound exam.

排除标准

  • Vulnerable patient- other than pediatric patients
  • Patients with ascites

结局指标

主要结局

Success rate of the spleen stiffness measurement (SSM) exam with both the optimized M+ probe and the exploratory XL+ probe, defined with at least 8 valid measurements after the exam quality control

时间窗: At baseline visit

The success rate is calculated with the number of valid measurements vs the total measurements done by the operator for every exam. The FibroScan will automatically analyze the measurement and based on some validity criteria will define the measurement as "valid" (will lead to a reliable SSM measurement) or "invalid" (will lead to a non-reliable SSM measurement).

次要结局

  • Success rate of the spleen stiffness measurement (SSM) exam with the S probe, defined with at least 8 valid measurements after the exam quality control.(At baseline visit)
  • Change of the applicability with the Spleen Targeting Tool (STT) and the automatic depth adaptation mode enabled.(At baseline visit)
  • Success rate of the spleen stiffness measurement (SSM) exam with the optimized M probe, defined with at least 8 valid measurements after the exam quality control.(At baseline visit)

研究者

发起方
Echosens
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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