跳至主要内容
临床试验/NCT07491731
NCT07491731终止不适用

24024 - Clinical In-use Analyte Stability Study for 17 Parameters in Venous and Arterial Blood for PICO A and safePICO A

Radiometer Medical ApS3 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2025年10月7日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
43
试验地点
3
主要终点
In-use analyte stability in adult arterial and venous whole blood in PICO A and safePICO A for each parameter, measuring at five testing timepoints measured in minutes (t=0, t=10, t=20, t=30, t=45).

研究概览

简要总结

The purpose is to determine the in-use stability of 17 parameters (pH, pCO2, pO2, cNa+, cCa2+, cCl-, cK+, cGlu, cLac, ctHb, sO2, FMetHb, FCOHb, FO2Hb, FHHb, FHbF & ctBil) in adult arterial and venous whole blood drawn and stored in aspirating syringes (PICO A and safePICO A) measured on ABL90 FLEX PLUS analyzer.

The study aims to determine the in-use sample stability for up to 45 min at room temperature (18-25 °C) for arterial and venous blood sample analysis in the PICO A and safePICO A syringes for all 17 parameters.

详细描述

In-use analyte stability study for 17 parameters. The stability study is a 5 time-point study analyzing five (5) syringes at T = 0 min, 10 min, 20 min, 30 min and 45 min. after sample collection. Series of five (5) syringes are collected from each investigational device safePICO A and PICO A. Each type of syringe will be analyzed on one ABL90 Flex Plus analyzer and for both types of blood (Arterial or Venous). For each syringe type a minimum of 50 + 7 series (7 contrived series) with samples within the reportable ranges will need to be tested for each blood type.

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

  • Subjects must meet all the criteria listed below to be eligible for participation in the study.
  • Subject must be 18 years of age or older.
  • Subject must have an arterial and/or venous line established as a part of the standard of care.
  • Subject evaluated by the principal investigator or designee as suitable for the study according to the protocol.

排除标准

  • Subjects meeting any of the criteria listed below will not be eligible for participation in the study.
  • Subjects, who are pregnant or breastfeeding.
  • Subjects who have been previously enrolled into this study.
  • Subjects exposed to following substances within the last 72 hours:
  • Acetylsalicylic Acid Sodium Salt at dose equal or above 1 gram/day
  • Acetylcysteine
  • Fluorescein dye
  • Patent Blue dye

结局指标

主要结局

In-use analyte stability in adult arterial and venous whole blood in PICO A and safePICO A for each parameter, measuring at five testing timepoints measured in minutes (t=0, t=10, t=20, t=30, t=45).

时间窗: One subject delivers blood samples to be measured over time (45 min.)

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)

Loading locations...

相似试验