跳至主要内容
临床试验/NCT02854345
NCT02854345已完成不适用

Preliminary Study Concerning the Validity of Parathyroid Exploration on a Discovery NM 530c CZT Camera

Centre Hospitalier Universitaire de Besancon1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2014年9月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1
主要终点
Comparison of pathologic parathyroid detection performances between planar pinhole on Anger camera and tomoscintigraphy on CZT camera, gold standard being the pathological results after surgery

研究概览

简要总结

The goal of this study is to assess the performance of parathyroid imaging on a cardiac-dedicated CZT camera, compared to planar pinhole imaging, in patients referred for primary hyperparathyroidism.

详细描述

The goal is to determine if parathyroid tomoscintigraphy on a CZT camera can provide at least equivalent diagnostic performance, compared with planar pinhole imaging.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •suffering from sporadic primary hyperparathyroidism
  • •referred to the Nuclear Medicine Dept for a pre-operative scintigraphy of the parathyroid glands
  • •who have given their written consent
  • •who benefit from the French Government Medical Insurance

排除标准

  • •pregnant women
  • •ages < 18 or > 80 years
  • •hyperparathyroidism recidive after a first surgery
  • •secondary or tertiary hyperparathyroidism
  • •Multiple endocrine Neoplasia (MEN) type I context or familial history of hyperparathyroidism
  • •absence of written consent
  • •non-beneficiary of the French Government Medical Insurance

研究组 & 干预措施

Tomoscintigraphic parathyroid imaging on a CZT camera

Experimental

Tomoscintigraphic parathyroid imaging on a CZT camera

干预措施: Tomoscintigraphic parathyroid imaging on a CZT camera (Device)

结局指标

主要结局

Comparison of pathologic parathyroid detection performances between planar pinhole on Anger camera and tomoscintigraphy on CZT camera, gold standard being the pathological results after surgery

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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