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
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