跳至主要内容
临床试验/NCT03722459
NCT03722459
已完成
不适用

Novel MRI Sequence- MR Fingerprinting

University of North Carolina, Chapel Hill1 个研究点 分布在 1 个国家目标入组 22 人2018年11月2日
适应症Disease

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Disease
发起方
University of North Carolina, Chapel Hill
入组人数
22
试验地点
1
主要终点
Percent of Patients With Visible Region of Interest (Imaging Visibility)
状态
已完成
最后更新
3年前

概览

简要总结

Magnetic Resonance Imaging (MRI) has become one of most important medical imaging tools over the past 30 years because it is non-invasive, requires no ionizing radiation, and provides exquisite images of soft tissues and anatomic structures with many tissue/disease specific contrasts. While MRI has served the community well for many years, it is increasingly clear that it also has significant limitations.

One of the principle limitations is the lack of quantitative information for tissue/structure characterization. The current paradigm of MRI is to use a set of scanner settings to generate an image "weighted" by a specific MR contrast mechanism (physical parameter), where it is hoped that variations in the parameter will be accentuated. However, without quantitative knowledge of the parameters, the final image contrast may depend on many factors, which complicates image interpretation and diagnostic performance. Quantitative measurement can provide a great deal of information about tissue properties and pathological conditions, since these parameters ultimately determine the contrast that is observed in conventional images.

详细描述

The purpose of this study is to evaluate novel quantitative MRI techniques in clinical studies to determine whether they can provide better, faster and more useful information for clinical diagnosis. In this study, the investigators propose to apply MR Fingerprinting and evaluate its performance for different diseases. These include, but are not limited to, diseases in the liver, kidney, cardiac, pancreas etc. The investigators hypothesize that the quantitative MR Fingerprinting imaging technique will lead to improved tissue characterization and diagnosis.

注册库
clinicaltrials.gov
开始日期
2018年11月2日
结束日期
2022年9月9日
最后更新
3年前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

入排标准

入选标准

  • The study will include English-speaking patients that are already scheduled to undergo a clinical MRI for diagnostic purposes.

排除标准

  • Pregnant women will be excluded.
  • Women will be excluded from the healthy volunteers, due to a lack of funding for pregnancy testing. Funding for this will be considered for the future.

结局指标

主要结局

Percent of Patients With Visible Region of Interest (Imaging Visibility)

时间窗: Immediately following MRI completion, within approximately 5 minutes

MR fingerprinting sequences will be examined to determine their utility for visualizing pathology.

研究点 (1)

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