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临床试验/NCT03081767
NCT03081767已完成不适用

Comparison of Standard PET/CT vs. Digital PET/CT

Stanford University2 个研究点 分布在 1 个国家目标入组 199 人开始时间: 2017年3月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
199
试验地点
2
主要终点
Diagnostic Image Quality

研究概览

简要总结

The investigators wish to determine if standard and digital PET/CT scanners provide equivalent results for disease detection and diagnosis.

详细描述

There will be a single injection of the PET radiopharmaceutical followed by a standard PET/CT scan and immediately after by the digital PET/CT scan, or vice versa. The investigators wish to determine if image quality is equivalent with the digital PET/CT scanner.

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

入选标准

  • Patient is ≥ 18 years old at the time of the scan
  • Patient provides written informed consent
  • Patient is referred for standard (F18 FDG; F18 NaF; Ga68 DOTATATE) or research (68Ga PSMA or 68Ga RM2) PET/CT
  • Patient is capable of complying with study procedures
  • Patient is able to remain still for duration of imaging procedure (approximately 60 minutes total for both PET/CT)

排除标准

  • Patient is pregnant or nursing

结局指标

主要结局

Diagnostic Image Quality

时间窗: an expected average of 3 hours

Diagnostic image quality will be determined using a 5-point Likert Scale that reads: 5 - Diagnostic: Excellent diagnostic image quality; 4 - Diagnostic: Good diagnostic image quality; 3 - Diagnostic: Acceptable diagnostic image quality; 2 - Sub-optimal diagnostic: image quality with limited additional clinical information; 1 - Non-diagnostic: non-diagnostic image quality

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Andrei Iagaru

Chief of the Division of Nuclear Medicine and Molecular Imaging

Stanford University

研究点 (2)

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