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临床试验/NL-OMON31922
NL-OMON31922已完成不适用

on invasive imaging of [18F] HX-4 with Positron-Emission-Tomography (PET): A phase I trial - HX4-fase I

MAASTRO clinic0 个研究点目标入组 12 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Histological or cytological confirmed solid tumour, primary or secondary stage IV and/ or tumours with no curative treatment options.
  • - WHO performance status 0 to 1
  • - Normal white blood cell count and formula
  • - Normal platelet count
  • - No anaemia requiring blood transfusion or erythropoietin
  • - Adequate hepatic function.
  • - Calculated Creatinin clearance at least 60 ml/min
  • - No administration of Fluor-18 in the previous 24 hours
  • - The patient is capable of complying with study procedures
  • - 18 years or older

排除标准

  • - Recent (< 3 months) myocardial infarction
  • - Uncontrolled infectious disease
  • - Less than 18 years old
  • - pregnant by testing patient with a serum or urine test within 24 hours of receiving 18F-Hx4
  • - No concurrent anti-cancer agents or radiotherapy allowed.

研究者

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