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临床试验/NCT04146246
NCT04146246已完成不适用

Comparative Evaluation of the FINDERTM Instrument and FINDERTM G6PD Cartridge in Adults and Neonates

Baebies, Inc.3 个研究点 分布在 1 个国家目标入组 119 人开始时间: 2019年11月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
119
试验地点
3
主要终点
G6PD enzymatic activity in adults and neonates

研究概览

简要总结

A prospective clinical study to compare the clinical performance of the FINDER™ Instrument and the G6PD assay to an FDA cleared instrument/reagent combination in adult and neonate populations.

详细描述

A prospective clinical study to compare the clinical performance of the FINDER™ Instrument and the G6PD assay to an FDA cleared instrument/reagent combination in adult and neonate populations. Neonate and adult subjects will be recruited from 3 clinical sites. Neonate samples will be collected as heel prick unless an in dwelling line is already in place at which point a venous or arterial/umbilical sample will be collected. Adult samples will be collected as venous/arterial samples and finger stick samples. Samples will be tested at the point of care/near patient and in the clinical laboratory using the FINDER Instrument and G6PD assay on a digital microfluidic platform. Samples will also be sent to a third party CLIA laboratory for test using an FDA 510(k) cleared instrument/reagent combination for G6PD.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
35 Weeks 至 100 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Neonates aged >35 gestational weeks or older.
  • Adult subjects who are age 18 and older.
  • Adult subjects who weigh at least 110 pounds.
  • All ethnicities.
  • Male and female subjects.

排除标准

  • Adult subjects who weigh less than 110 pounds.
  • Subjects with anemia for which an attending physician will not authorize a blood draw.
  • Subjects who have received a blood transfusion.
  • Subjects who are pregnant.

结局指标

主要结局

G6PD enzymatic activity in adults and neonates

时间窗: Immediately following a blood draw.

G6PD enzymatic activity in the FINDER System for adults and neonates compared to the G6PD activity tested using a known FDA cleared assay/instrument combination

次要结局

  • Point of care/near patient results and clinical laboratory results(Immediately following a blood draw.)
  • Arterial/venous whole blood results and tissue capillary test results(Immediately following a blood draw.)

研究者

发起方
Baebies, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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