临床试验/NCT01598766

NCT01598766Unknown1 期

General Investigational Protocol for EXCELART VANTAGE ZGV/XGV/AGV/ ATLAS/XGV/ZGV TITAN/XGV VANTAGE TITAN 3T

Toshiba America Medical Systems, Inc.2 个研究点分布在 1 个国家目标入组 100 人开始时间: 2012年5月最近更新: 2013年2月5日

适应症

试验速览

阶段: 1 期
发起方: Toshiba America Medical Systems, Inc.
入组人数: 100
试验地点: 2
主要终点: 16 Channel Flex Coil

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study is a feasibility study to evaluate new technology to improve the MRI experience, with coils, sequences and software. Patients from the Principle Investigator's exam schedule are given the opportunity to participate in this study is their MRI exam is appropriate for the specific coil, sequence or software being evaluated. If they agree, they can receive their MRI exam with the new coil, sequence or software instead of the standard one.

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: 6 Months 至 18 Years（Child, Adult）
性别: All
接受健康志愿者: 是

入选标准

•Pediatric patients that are scheduled for a clinically necessary MRI exam provided the subject meets the criteria of the department MRI screening procedure and their study is appropriate for the use of the 4 Channel Flex SPEEDER coil of the 16 Channel Metaflex SPEEDER coil.

排除标准

•Any contraindication to MRI procedures

结局指标

主要结局

16 Channel Flex Coil

时间窗: May 2012-May 2013

The 16 Channel Flex Coil will be evaluated for how well it performs on pediatric patients.

次要结局

8 Channel Value Breast Coil(6 months)

研究者

发起方

Toshiba America Medical Systems, Inc.

申办方类型

Industry

责任方

Sponsor

研究点 (2)

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