跳至主要内容
临床试验/NL-OMON55194
NL-OMON55194招募中不适用

on-Ionizing Metabolic Imaging using robust phosphorus MRI to predict treatment efficacy. - NIMI study

niversitair Medisch Centrum Utrecht0 个研究点目标入组 45 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
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
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Inclusion criteria for pancreatic cancer:
  • To be eligible to participate in this study, a subject must meet all of the
  • following criteria:
  • Patients with (borderline) resectable- or locally advanced pancreatic cancer,
  • with histological or cytological proof, scheduled for standard of care
  • chemotherapy containing fluorouracil, oxaliplatin, irinotecan and leucovorin
  • (FOLFIRINOX) as assessed by a medical oncologist.
  • Tumour size >= 1cm.
  • WHO-performance score 0-1, weight >=40kg
  • Written informed consent.
  • Inclusion criteria healthy volunteers (control group pancreas cohort):
  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • Healthy volunteers; No history of cancer, no history of chronic diseases, no
  • history of a pancreatic disease, no elective surgery <8 weeks
  • Age: >= 18yrs
  • WHO-performance score 0-2.
  • Written informed consent.
  • Inclusion criteria for lung cancer:
  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • Patients with non-small cell lung cancer, with histological or cytological
  • proof, scheduled for immune checkpoint inhibitors
  • Tumour size >= 2cm.
  • WHO-performance score 0-2, weight >=40kg
  • Written informed consent.

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • Any psychological, familial, sociological, or geographical condition
  • potentially hampering adequate informed consent or compliance with the study
  • Contra-indications for 7T MR scanning, including patients with a pacemaker,
  • cochlear implant or neurostimulator; patients with non-MR compatible metallic
  • implants in their eye, spine, thorax or abdomen; or a non-MR compatible
  • aneurysm clip in their brain; patients with claustrophobia and/or obesitas.

研究者

发起方
niversitair Medisch Centrum Utrecht

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