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临床试验/NCT07595666
NCT07595666Enrolling By Invitation不适用

Prospective Comparison of Ultra-high Resolution NeuroExplorer PET/CT Versus Standard-of-care PET/CT of the Head and Neck Region

prof. dr. Koen Van Laere1 个研究点 分布在 1 个国家目标入组 1,600 人开始时间: 2025年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
1,600
试验地点
1

研究概览

简要总结

The goal of this clinical study is to compare the current standard-of-care PET/CT scanner with the new NeuroEXPLORER PET/CT, with the aim of demonstrating the added diagnostic value of the new scanner. As this is the first device of its kind in Europe, the study will also evaluate the safety and general feasibility of the NeuroEXPLORER system for head and neck PET studies.

Due to to its high resolution, the NeuroEXPLORER enables an accurate investigation of areas up to 20 times smaller than what can be visualized with standard clinical PET scanners, providing images with a very high level of detail. This scanner is specifically designed for imaging the brain, spinal cord, and neck region, to support the diagnosis and monitoring of neurological, psychiatric, and other disorders in the head and neck.

The main questions this study aims to answer are:

  • Does the NeuroEXPLORER provide more detailed information with better diagnostic quality compared to standard clinical PET/CT scans for head and neck disorders?
  • Is the NeuroEXPLORER system safe and effective in performing head and neck studies?

Participants will:

  • receive clear information about the study, including its organization, possible risks, and potential benefits. Based on this, they will be able to give their informed consent by signing an informed consent form before the study begins.
  • visit the clinic (UZ Leuven) once for two consecutive PET/CT scans: first the prescribed clinical scan, followed by a shorter scan with the NeuroEXPLORER.
  • before the start of the regular PET/CT scan, have a small catheter placed in a blood vessel in the forearm. Through this, a tracer will be administered. A tracer is a small amount of slightly radioactive material that helps to produce images of processes inside the body. Depending on the tracer used, the PET/CT scan may start immediately or after a short waiting period.
  • lie on their back on the scanner bed for 10 to 30 minutes during the clinical scan.
  • after the clinical scan, undergo a 15-20 minute scan on the NeuroEXPLORER.
  • leave the hospital after completing both scans.
  • afterwards, be asked whether they experienced any discomfort during the study. In addition, they will receive a one-time follow-up phone call within a week after the scan to check if they experienced any discomfort in the days following the study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
28 Days 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All subjects referred for standard-of-care PET in the indications for the substudies are eligible.

排除标准

  • Subject is unwilling to avoid unusual, unaccustomed, or strenuous physical activity beginning 4 days prior to tracer injection up to 1 day after tracer injection.
  • Subject does not understand the study procedures.
  • Subject is unwilling or unable to perform all of the study procedures or is considered unsuitable in any way by the principal investigator.
  • Subject has had exposure to ionizing radiation (> 1 mSv) in other research studies within the last 12 months.
  • Subject does not agree that incidental findings are communicated to the general practitioner and to the participant him/herself.
  • Incapacitated patients that cannot give consent by themselves (in particular for substudies 1-3 in neurodegeneration).

研究者

发起方
prof. dr. Koen Van Laere
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

prof. dr. Koen Van Laere

Prof. dr. Koen Van Laere

Universitaire Ziekenhuizen KU Leuven

研究点 (1)

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