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临床试验/JPRN-jRCTs032190083
JPRN-jRCTs032190083招募中未知

Efficacy of Irreversible electroporation (IRE) on patients with hepatocellular carcinoma who are not eligible for liver resection and radiofrequency ablation (RFA): a multicenter trial

Sugimoto Katsutoshi0 个研究点目标入组 45 人开始时间: 2019年8月27日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • 1)Male and female with older than or equal to 20-year-old
  • 2)Patients who are pathologically proven or radiologically diagnosed hepatocellular carcinoma (HCC)
  • 3)Patients with HCC who meet Milan criteria (one lesion smaller than 5 cm; alternatively, up to 3 lesions, each smaller than 3 cm)
  • 4)Patients who are not eligible for liver resection and radiofrequency ablation
  • 5)Presence or absence of pretreatment is not essential qualification; but it is necessary that at least more than 4 weeks has passed since previous treatment
  • 6)Patients with Child-Pugh score less than or equal to 9
  • 7)Patients with ECOG performance status of 0 to 2
  • 8)Patients preserved adequate bone morrow, liver and kidney functions, as shown below:
  • White blood cell: >2,000 /mm3, and/or <10,000 /mm3
  • Platelet: >50,000 /mm3
  • Hemoglobin: >8.0 g/dL
  • Serum total bilirubin: <2.0 mg/dL
  • eGFR: >45 ml/min/1.73m2
  • BUN: <35 mg/dL
  • 9)Patients who have obtained agreements for participation in writing

排除标准

  • 1)Patients who have active double cancer (synchronous double cancer) or who have metachronous double cancer within five years disease duration: note that carcinoma in situ which is judged to be cure is not included
  • 2)Patient who have diagnosed as myocardial infarction, unstable angina, cardiac failure, and arrhythmia with care within 6 months before registration
  • 3)Patients who are difficult to be secured of safety percutaneous approach
  • 4)Patients who use pacemakers
  • 5)Patients who have iodine allergies, decline in renal function (eGFR<45ml/min/1.73m2), and cannot undertake contrast-enhanced CT for any reasons
  • 6)Patients who are judged to be difficult to undergo this clinical trial due to psychiatric disease or psychological symptom
  • 7)Patients who are in pregnancy or probable of pregnancy
  • 8)Besides, patients who are judged as inappropriate for registration by doctor in charge

研究者

发起方
Sugimoto Katsutoshi

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