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临床试验/NCT01667172
NCT01667172已完成不适用

Study of Technical Accuracy and Userfriendliness of Two Point-of-care C Reactive Protein Devices

KU Leuven6 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2012年4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
KU Leuven
入组人数
300
试验地点
6
主要终点
technical accuracy

研究概览

简要总结

Study to test technical accuracy and userfriendliness of two Point-of-care C Reactive Protein devices (POC CRP devices) in comparison with laboratory CRP testing on children and adults.

Research questions:

  1. Are the POC CRP devices technically accurate? Do the measured values agree with CRP values measured at the clinical laboratory?
  2. Are the 2 POC CRP devices equivalent ? 2.1. Are the 2 POC CRP devices equally reliable? 2.1.1. Comparison of 2 measurements in the same patient on 1 device (inter-observer-variability) 2.1.2. Comparison of 2 measurements in the same patient on 2 identical devices (inter-device-variability) 2.2. Are the 2 Point-of-Care CRP devices equally userfriendly in a general practice surgery? (userfriendliness

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
Double (Participant, Care Provider)

入排标准

年龄范围
1 Month 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • children: aged 1 month to 14 years
  • adults: aged 18-65 years

排除标准

  • children and adults not understanding Dutch language

结局指标

主要结局

technical accuracy

时间窗: 3 months

correlation obtained between the results from the Point-of-care C Reactive Protein devices and the results from the laboratory

次要结局

  • User-friendliness(3 months)
  • Inter-device variability(3 months)
  • Inter-observer variability(3 months)

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jan Verbakel

Research Assistant

KU Leuven

研究点 (6)

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