跳至主要内容
临床试验/NCT05060250
NCT05060250进行中(未招募)不适用

Symphony IL-6 Cutoff Establishment Study for Patients at Risk of Severe Sepsis

Bluejay Diagnostics, Inc.1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2021年8月31日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
96
试验地点
1
主要终点
Measurement of IL-6 Concentration in Patients at High Risk of Severe Sepsis

研究概览

简要总结

Symphony IL-6 is a device that quantitates human IL-6 by fluorescence enzyme immunoassay (FEIA) from whole-blood specimens. Use of Symphony IL- 6 removes the need for plasma separation before testing. Symphony IL-6 comprises two components, the Symphony Fluorescence Immunoanalyzer and the Symphony IL-6 Cartridge. Whole blood is added to the cartridge and then up to six cartridges can be inserted into the immunoanalyzer. After 20 minutes a readout and printout are given with a quantitative IL-6 concentration. The used cartridges are fully enclosed and can be easily disposed of in general hospital bio-waste. Given the nature of this device and its portability, there is potential for future deployment as a point-of-care (POC) device.

This study is to establish an interleukin-6 (IL-6) cutoff value using the Symphony IL-6 test for patients at high risk of severe sepsis caused by a COVID-19 infection.

研究设计

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

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Whole-blood specimen collected in K2 EDTA anticoagulant tubes
  • Subject is considered to have severe or critical illness per below:
  • Severe Illness
  • SpO2 < 94% on room air at sea level;
  • Ratio of arterial partial pressure of oxygen to fraction of inspired oxygen (PaO2/FiO2) < 300 mmHg;
  • Respiratory frequency > 30 breaths/min;
  • Or lung infiltrates >50% Critical Illness
  • a) Respiratory failure; b) Septic shock; c) And/or multiple organ dysfunction d) At least one criterion of severe illness
  • Subject confirmed to be COVID-19 positive by an EUA RT-PCR test
  • Subject is 18+ years of age
  • Minimum volume of 100µL for Symphony IL-6 testing
  • Specimen is available for testing within 12 hours from collection

排除标准

  • Subject is receiving an anti-IL-6 treatment
  • Subject is receiving corticosteroids
  • Hemolyzed specimens

结局指标

主要结局

Measurement of IL-6 Concentration in Patients at High Risk of Severe Sepsis

时间窗: Specimen is tested within 12 hours from collection

Determine the interleukin-6 concentration in whole blood samples from patients with confirmed COVID-19 infection and are at high risk of septic shock.

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 (1)

Loading locations...

相似试验