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临床试验/NCT06579833
NCT06579833进行中(未招募)不适用

Histotripsy (HistoSonics®) for Liver Tumours: a Phase II Safety and Efficacy Study

The University of Hong Kong2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年8月29日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
60
试验地点
2
主要终点
Changes in tumour features

研究概览

简要总结

Histotripsy is a promising non-invasive technique that uses high-intensity ultrasound waves to disrupt tissue without damaging surrounding structures. It works by using high-intensity ultrasound waves to create microscopic bubbles within the tumour tissue. These bubbles rapidly expand and collapse, generating shock waves that disrupt the tissue. The technique is highly precise and can be targeted to specific areas of the liver, allowing for selective destruction of tumour cells while minimizing damage to healthy tissue. This study will enrol 20 patients with liver tumours (be it primary or secondary liver tumours), monitor their post-operative adverse events, and study the changes in tumour size and volume after treatment. Histotripsy will be performed under general anaesthesia, with real-time monitoring by ultrasound, and deliver high-intensity ultrasound waves in single session or multiple sessions. Similar to other minimal invasive treatments, patients will be admitted 1 day prior, then receive Histotripsy on the next day and stay overnight for observation. Patients will be discharged on the 3rd day if unremarkable. During the hospital stay, blood samplings will be taken for evaluation around 2-4 times in total depending on the length of hospital stay.

研究设计

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

  • Fit for general anaesthesia
  • Liver tumour size < 10cm
  • Solitary or multifocal
  • Primary liver tumour such as hepatocellular carcinoma or intrahepatic cholangiocarcinoma
  • Secondary liver tumour such as liver metastasis
  • Patients with operable or inoperable liver tumours
  • Liver transplant candidates awaiting for liver graft

排除标准

  • Refusal to take part in clinical trial
  • Child C liver cirrhosis
  • Not fit for general anaesthesia

结局指标

主要结局

Changes in tumour features

时间窗: up to 36 months

Changes in tumour size and volume before and after intervention

Post procedure adverse events and complication

时间窗: The whole duration of hospital stay, normally 3 days on average

Post procedure adverse events and complication

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Albert Chi Yan Chan

Clinical Professor

The University of Hong Kong

研究点 (2)

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