跳至主要内容
临床试验/NCT00593541
NCT00593541终止不适用

Development of New Software Capabilities for Use With Cardiovascular Magnetic Resonance Imaging

University of California, Davis0 个研究点目标入组 42 人开始时间: 1999年5月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
42
主要终点
Extend or generalize certain capabilities, such as new data acquisition pulse sequences, new image processing and analysis software for structural and functional analysis of the MR images

研究概览

简要总结

This Protocol is intended to facilitate development and testing of new cardiovascular MRI software capabilities by UC Davis Research Faculty, as well as to facilitate the evaluation of new software capabilities provided by GE and Siemens.

详细描述

This protocol will permit normal subjects, as well as patients with suspected or proven medical conditions, to undergo MRI studies using the new software capabilities. This Protocol is not restricted to imaging of a particular organ system or disease. The Protocol does not involve injection of any contrast agent, or other minimally-invasive or invasive procedure. It is intended only for those cases for which the only requirement of the subject is to relax and lie still while imaging is being performed.

研究设计

研究类型
Observational
观察模型
Case Control
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

  • 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

结局指标

主要结局

Extend or generalize certain capabilities, such as new data acquisition pulse sequences, new image processing and analysis software for structural and functional analysis of the MR images

时间窗: Post-scanning

次要结局

  • Improve image quality by various techniques (e.g. reducing the effects of motion)(Post-scanning)

研究者

申办方类型
Other
责任方
Sponsor

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