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临床试验/NCT02071706
NCT02071706已完成不适用

Clinical Evaluation of an Integrated PET/MRI System

GE Healthcare2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2014年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
GE Healthcare
入组人数
62
试验地点
2
主要终点
Number Usable PET/MRI Image Sets

研究概览

简要总结

The investigational PET/MRI scanner, including attenuation correction method, is capable of producing diagnostic quality images and appropriate device functionality per user feedback.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

入选标准

  • Subject must have a clinical indication for a PET/CT exam
  • Subject must be at least eighteen (18) years of age; and
  • Female subjects that are determined to be non-pregnant by a physician investigator or are demonstrated non-pregnant by negative urine pregnancy test administered within the 24 hour period before PET/CT imaging; and
  • Subject must be able to hear and understand instructions without assistive devices; and
  • Subject must provide written informed consent; and
  • Subject has the necessary mental capacity to understand instructions, and is able to comply with protocol requirements; and
  • Subject is able to remain still for duration of imaging procedure (approximately 60 minutes total for PET/MRI); and
  • Subject must be able to participate in a PET/MR imaging session within 2 hours of concluding their PET/CT exam and within 4 hours of PET radiotracer administration.

排除标准

  • Subjects who have any axial diameter larger than 55 cm; or
  • Subjects with a weight greater than 227 kgs; or
  • Subjects that have metallic/conductive or electrically/magnetically active implants without MR Safe or MR Conditional labeling, with the exception of dental devices/fillings, surgical clips, and surgical staples determined to be safe for MRI scanning by a physician investigator; or
  • Subjects that have implants with MR Unsafe labeling; or
  • Subjects that have implants labeled as MR Conditional by the manufacturer for which the allowable conditions are not expected to be achieved by the MR/PET environment or scan protocol ; or
  • Subjects who have a contraindication to MRI according to the screening policy of the participating site

研究组 & 干预措施

Single-Arm PET/MRI

Other

Single-group evaluation of PET/MRI for diagnostic quality of image

干预措施: PET/MRI system (Device)

结局指标

主要结局

Number Usable PET/MRI Image Sets

时间窗: 1 day

The number PET/MRI image sets determined usable by a radiologist on a yes/no binary scale

Number of Diagnostic Quality Images

时间窗: 1 day

Number of images sets deemed diagnostic quality by the investigator

次要结局

未报告次要终点

研究者

发起方
GE Healthcare
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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