跳至主要内容
临床试验/NCT00593931
NCT00593931终止不适用

Development Of New Techniques For Functional Magnetic Resonance Imaging Of The Brain

University of California, Davis0 个研究点目标入组 215 人开始时间: 1999年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
215
主要终点
transient changes in blood flow in the brain that occurs with neuronal activity

研究概览

简要总结

This Protocol is intended to facilitate development and testing of new techniques for functional MRI by UC Davis Research Faculty, as well as to facilitate the evaluation of new techniques provided by the system manufacturers (GE and Siemens).

详细描述

New techniques covering a wide range of clinical and scientific applications will be developed, tested and evaluated. These include 1. Investigation of sensory stimulus processing and cognitive processing, both in normal subjects and patients with psychiatric disorders, 2. Early detection of stroke and other ischemic injury, and 3. Characterization of tumor distribution and activity. The new techniques will routinely need to be tested with respect to the following: 1. Sensitivity to blood oxygenation versus blood flow versus blood volume contrast mechanisms, 2. Signal-to-noise and contrast-to-noise ratio, 3. Spatial and temporal resolution, 4. Distribution and severity of image artifacts, and 5. Duty cycle limitations. Most clinical applications will require coverage of the entire brain and consequently high duty cycle operation, which needs to be traded off with spatial and temporal resolution, as well as contrast mechanisms. The work will also involve the testing of different experimental paradigms (time sequence of stimuli or cognitive tasks) to identify that which provides the highest signal change associated with the specific brain activity of interest.

Although 3T provides twice the signal of 1.5T systems, for some research applications this image quality advantage of 3T may be outweighed by other effects of higher field on the signal. Consequently, most new techniques will be evaluated on both the 1.5T and 3T systems, and a decision will be made based upon the overall image quality, regarding which system is to be used.

The Protocol does not involve injection of any contrast agent or drug, or other minimally-invasive or invasive procedure. It is intended specifically for those studies in which the subject is required, in addition to trying to relax and lie still, only to experience and respond to various non-harmful sensory stimuli, or to perform common cognitive (e.g. math calculations) and or motor (e.g. finger tapping) tasks.

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

入选标准

  • •18 years of age or older
  • •ability to give informed, written consent
  • •Not pregnant or breastfeeding

排除标准

  • •Electrically, magnetically, or mechanically activated implants (for example, cardiac-pacemakers)
  • •Ferromagnetic implant, such as an aneurysm clip, surgical clip, or prosthesis
  • •History of uncontrolled claustrophobia

研究组 & 干预措施

A

Experimental

Normal Subjects

干预措施: fMRI (Other)

结局指标

主要结局

transient changes in blood flow in the brain that occurs with neuronal activity

时间窗: Post-scanning

次要结局

  • Sensitivity to blood oxygenation versus blood flow versus blood volume contrast mechanisms(Post-scanning)

研究者

申办方类型
Other
责任方
Sponsor

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