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临床试验/NCT02897154
NCT02897154已完成不适用

Clinical Evaluation of i-STAT Analyzer for Glucose, Hematocrit and Sodium

Abbott Point of Care3 个研究点 分布在 1 个国家目标入组 297 人开始时间: 2016年5月10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
297
试验地点
3
主要终点
Glucose (mg/dL) levels

研究概览

简要总结

The objective of this study is to compare the performance of two i-STAT Analyzers in a Point-of-Care (POC) setting. The evaluation will be performed using a cartridge to test glucose, hematocrit and sodium on capillary specimens.

详细描述

The clinical performance for glucose, hematocrit and sodium assays for capillary samples was evaluated for the investigational i-STAT 500 (Alinity) analyzer based on results of method comparison testing against the i-STAT 1W analyzer.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

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

  • Subject is ≥ 18 years of age
  • Subjects (or their legal representative) who are willing to voluntarily consent to the study

排除标准

  • There are no exclusion criteria

结局指标

主要结局

Glucose (mg/dL) levels

时间窗: Patient's blood is tested within 3 minutes of blood collection

Data analysis

Hematocrit (%PCV) levels

时间窗: Patient's blood is tested within 3 minutes of blood collection

Data analysis

Sodium (mmol/L) levels

时间窗: Patient's blood is tested within 3 minutes of blood collection

Data analysis

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (3)

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