Histotripsy (HistoSonics®) for Liver Tumours: a Phase II Safety and Efficacy Study
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
- 否
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
Albert Chi Yan Chan
Clinical Professor
The University of Hong Kong
