跳至主要内容
临床试验/NCT03677999
NCT03677999撤回不适用

Spectroscopic Magnetic Resonance Imaging of Glioma

University of Minnesota1 个研究点 分布在 1 个国家目标入组 304 人开始时间: 2019年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
304
试验地点
1
主要终点
The number of brain cancer participants with IDH mutation status

研究概览

简要总结

The study is designed to develop and test new Magnetic Resonance Imaging methods that can improve the characterization of brain cancer and facilitate improved clinical care of these participants.

详细描述

The primary objective of this study is to develop and test new Magnetic Resonance Imaging methods that can improve the characterization of brain cancer and facilitate improved clinical care of these participants. More specifically, investigators are interested in applying novel spectroscopic and quantitative MR methods that give information beyond what is produced by a clinical brain MRI study and to understand the clinical correlates of the imaging findings. Investigators have tested these sequences in healthy volunteers. The investigators now wish to test these sequences in brain cancer participants in order to understand how these sequences can best be applied in a clinical setting.

To acquire these data, investigators intend to perform additional MRI acquisitions on participants who are scheduled to receive a clinical MRI at the UMN Center for Clinical Imaging Research (CCIR), a facility located at the Center for Magnetic Resonance Research (CMRR). Since these MRIs are required for the participants' clinical care, the participant will not be making additional visits to the CCIR. Based on published data and pilot experiences reported from other institutions, the sequences are well-tolerated. The only imposition for the participant is that the participant will spend additional time in the scanner after completion of the imaging required for clinical care. An informed consent form describing the additional MR sequences performed will be presented to the participant.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women scheduled who are diagnosed with glioma who is seeking clinical care for their conditions at the UMN Masonic cancer center.
  • Passed the safety screen for MRI
  • Age 18 or older
  • Ability to read and understand English
  • Ability to provide informed consent

排除标准

  • Participants who are excluded from the base MRI scan, as determined by the CMRR/CCIR clinical policies are necessarily excluded from this study, as the MRI scan will not be performed.
  • Pregnant women

结局指标

主要结局

The number of brain cancer participants with IDH mutation status

时间窗: 30 minutes

MEGA-PRESS MRI sequence will be utilized to determine IDH status

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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