跳至主要内容
临床试验/NCT02529137
NCT02529137已完成不适用

Pivotal Study for Validation of Philips Dx for Diagnosis in Surgical Pathology

Philips Digital & Computational Pathology4 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2015年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
2,000
试验地点
4
主要终点
Major Discordance Rate

研究概览

简要总结

The primary objective of this study is to show safety and effectiveness of the PDx for In Vitro Diagnostic (IVD) use as an aid to the pathologist to view, review and diagnose digital images of surgical pathology slides.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Major Discordance Rate

时间窗: 6 months

The primary endpoint was the difference in major discordance rates between Manual Optical (MO) and Manual Digital (MD). MO is defined as reading by using optical microscope whereas MD is defined as reading by using PIPS. MO major discordance rate is defined as the proportion of major discordances between the MO diagnosis and the main diagnosis from the total number of readings. MD major discordance rate is defined as the proportion of major discordances between the MD diagnosis and the main diagnosis from the total number of readings.

次要结局

未报告次要终点

研究者

发起方
Philips Digital & Computational Pathology
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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