跳至主要内容
临床试验/JPRN-jRCTs031220192
JPRN-jRCTs031220192招募中2 期

Safety and pharmacokinetic study of a new PET probe [18F]FEDAC in patients with suspected malignant tumors

Tamura Kentaro0 个研究点目标入组 30 人开始时间: 2022年7月7日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
30

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.Subjects who are 18 years of age or older at the time of consent acquisition
  • 2.Subjects who have been confirmed to have malignant tumors by histopathological examination performed within the past 90 days from the date of consent acquisition or by diagnostic imaging within the past 28 days from the date of consent acquisition
  • 3.Subjects whose Performance Status (ECOG PS) is 0 or 1
  • 4.Subjects who provide written informed consen

排除标准

  • 1.Subjects who have severe or progressive complications or subjects who have a history of these complications and are judged by the investigator or co-investigator to be unsuitable for this study
  • 2.Subjects who have obvious abnormalities in physical and laboratory examinations (blood test and urine test) after obtaining the informed consent
  • 3.Subjects with drug addiction or alcohol addiction
  • 4.Subjects with mental illness or psychiatric symptoms who are judged to have difficulty in participating in this study
  • 5.Subjects who are unable or restricted from the tests specified in the research plan
  • 6.Subjects who are claustrophobic
  • 7.Subjects who is considered to be inappropriate to participate in this study by the investigator or co-investigator

研究者

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