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临床试验/JPRN-jRCTs062220088
JPRN-jRCTs062220088招募中2 期

A study on the efficacy of preoperative marking for liver tumors difficult to identify intraoperatively

Ohdan Hideki0 个研究点目标入组 25 人开始时间: 2023年1月25日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
25

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • 1.Patients who are already scheduled for percutaneous biopsy or contrast-enhanced catheterization for diagnostic purposes of liver tumor or liver tissue.
  • 2.Patients scheduled for hepatic resection for liver tumor.
  • 3.Patients with Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0-1.
  • 4.Male or female patients (regardless of outpatient or inpatient status) who are at least 18 years of age at the time of consent.
  • 5.Patients with clear tumor lesions in the liver on CT, MRI, or other imaging studies. The number of tumors is not specified.
  • 6.Patients with no intervening organs in the puncture pathway and who are considered to be able to be punctured safely under CT or ultrasound guidance.
  • 7.Patients who meet the following criteria in blood tests at the time of enrollment and whose major organs (bone marrow, liver, kidney, lungs, etc.) are still functional.
  • A) White blood cell count: 2,000/mm3 or higher
  • B) Hemoglobin level: 8.0 g/dL or higher
  • C) Platelet count: 50,000/mm3 or higher
  • D) Total bilirubin: 3.0 mg/dL or less
  • 8.Patients who have sufficient judgment to understand the content of the study and have given written consent to participate in this study.
  • 9.Patients who are able to take a break from anticoagulants on the day of marking.

排除标准

  • 1.Patients with severe ischemic heart disease (NYHA classification III or higher).
  • 2.Patients with severe hepatic cirrhosis (hepatic impairment level C).
  • 3.Patients with dyspnea requiring oxygen administration due to interstitial pneumonia or pulmonary fibrosis.
  • 4.Patients on dialysis for chronic renal failure.
  • 5.Patients with active multiple cancers who are currently undergoing treatment.
  • 6.Patients with psychosis or psychiatric symptoms that make it difficult for them to participate in the study.
  • 7.Patients who are deemed inappropriate to participate in the study by the principal investigator or subinvestigator.
  • 8.Patients with hypersensitivity to platinum alloys.

研究者

发起方
Ohdan Hideki

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