NCT03457506已完成不适用
Intra-individual Patient-based Comparison of Conventional and Digital PET/CT Scanners
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Isala
- 入组人数
- 225
- 试验地点
- 1
- 主要终点
- Diagnostic outcome of the PET/CT study
研究概览
简要总结
In this study, the investigators will analyze the impact of digital PET/CT on the final diagnostic conclusion of the scan in patients with lung cancer, breast cancer, esophageal cancer and a group of mescellaneous cancers.
详细描述
There will be a single injection of the PET radiopharmaceutical FDG, followed by a conventional PET/CT scan and a digital PET scan, in this order or vice versa.
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
- 否
入选标准
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •referred to Isala for a clinically indicated FDG-PET/CT scan
- •suspected or proven lung cancer, esophageal cancer, breast cancer or miscellaneous cancer, either as a primary diagnosis or follow-up study
- •signed informed consent
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •age < 18 years
- •incapacitated adults
- •prisoners
- •pregnant patients
- •unable to undergo two consecutive PET/CT scans
研究组 & 干预措施
Patients undergo a digital PET/CT
Other
Single arm prospective study of paired PET scans. Patients who are referred to the nuclear medicine department to undergo a PET scan, will undergo a PET/CT scan on the conventional scanner as well as the digital PET/CT scanner.
干预措施: Digital PET/CT scan (Diagnostic Test)
结局指标
主要结局
Diagnostic outcome of the PET/CT study
时间窗: approximately 2 hours
次要结局
- PET image quality(approximately 2 hours)
研究者
研究点 (1)
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