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临床试验/NCT07815054
NCT07815054尚未招募不适用

Efficacy Evaluation of Microwave Ablation Assisted by Diaphragm Hydrodissection for Hepatocellular Carcinoma and Comparative Analysis With Surgical

The First Hospital of Jilin University0 个研究点目标入组 200 人开始时间: 2026年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
200
主要终点
Progression-free survival (PFS)

研究概览

简要总结

The goal of this observational study is to evaluate the local efficacy and safety of hydrodissection-assisted microwave ablation for patients with hepatocellular carcinoma, and to compare its therapeutic outcomes with surgical resection for hepatocellular carcinoma. The main questions it aims to answer are:

Is hydrodissection-assisted microwave ablation safe and effective for treating hepatocellular carcinoma? How does the therapeutic effect of hydrodissection-assisted microwave ablation compare with surgical resection for hepatocellular carcinoma? Patients who receive either microwave ablation or surgical resection will Undergo a 2-year follow-up period.

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Patients with Child-Pugh grade A or B liver function.Single hepatic lesion with a maximum diameter ≤ 5 cm.The lesion is located in the subphrenic region with a distance ≤ 10 mm from the right diaphragm.

排除标准

  • Presence of extrahepatic metastasis or other concomitant malignant tumors.Presence of severe cardiac, pulmonary, or renal dysfunction.Platelet count < 50×10⁹/L with irreversible coagulation disorders. Patients with incomplete imaging or clinical medical data.

研究组 & 干预措施

Hydrodissection-assisted microwave ablation cohort

Patients with hepatocellular carcinoma receiving hydrodissection-assisted microwave ablation under routine clinical care. No study-specific intervention will be assigned by researchers.

干预措施: Microwave Ablation Assisted by Diaphragm Hydrodissection (Procedure)

Surgical resection cohort

Patients with hepatocellular carcinoma receiving surgical resection under routine clinical care. No study-specific intervention will be assigned by researchers.

干预措施: Surgical Resection (Procedure)

结局指标

主要结局

Progression-free survival (PFS)

时间窗: Up to 2 years after treatment

the time from initiation of treatment to disease progression or death.

次要结局

  • Overall survival (OS)(Up to 2 years after treatment)

研究者

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

Dezhi Zhang

Associate Chief Physician,Abdominal Ultrasound Department

The First Hospital of Jilin University

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