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临床试验/NCT05492227
NCT05492227已完成不适用

SARS-CoV-2 Nucleic Acid Detection Kit

TransGen Biotech Co., LTD1 个研究点 分布在 1 个国家目标入组 607 人开始时间: 2022年7月5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
607
试验地点
1
主要终点
Sensitivity of the SARS-CoV-2 NAD Kit

研究概览

简要总结

SARS-CoV-2 Nucleic Acid Detection Kit is an In Vitro Diagnostic (IVD) medical device intended for RNA detection of SARS-CoV-2 in human specimens using multiplex real-time polymerase chain reaction (RT-PCR) technology. The conserved regions of ORF1ab and N genes are used as target sites of the primers and probes according to the indications provided in the Instructions for Use (IFU).

详细描述

The SARS-CoV-2 Nucleic Acid Detection Kit is an In Vitro Diagnostic (IVD) medical device intended for Qualitative RNA detection of SARS-CoV-2 using multiplex real time RT-PCR technology for professional use. The kit is available in two different formats (48 tests/kit or 200tests/kit), and it can be stored at -20±5ºC away from light for 12 months. This kit includes a PCR Reaction Mix, PCR Enzyme Mix, SARS-CoV-2 PCR Primer/Probe Mix and a negative/positive control.

TransGen SARS-CoV-2 Nucleic Acid Detection Kit is intended for in vitro qualitative detection of ORF1ab and N genes from the SARS-CoV-2 virus in nasopharyngeal swab specimens collected from COVID-19 suspected cases, suspected clusters of cases or other individuals who need SARS-CoV-2 infection diagnosis or differentiation diagnosis. The definitions of COVID-19-related groups, such as "suspected cases" or "suspected clusters of cases", are detailed in the Diagnosis and Treatment Protocol for Novel Corona virus Pneumonia, Surveillance Protocol for Novel Corona virus Pneumonia or other COVID-19 documents from the Centers for Disease Control and Prevention (CDC). The TransGen SARS-CoV-2 Nucleic Acid Detection Kit should comply with the requirements of Diagnosis and Treatment Protocol for Novel Corona virus Pneumonia, Protocol for Prevention and Control of COVID-19 and other COVID-19 documents from the CDC. The biosafety requirements should be strictly followed as well.

Specimens used for this clinical performance study will be remnants of specimens taken for purposes of standard of care (leftover or archived) through a nasal swab from male and female subjects. Specimens may come from persons suspected of SARS-CoV-2 infection but also from those who need a diagnostic test due to other reasons such as medical intervention, blood donors, or travel for which a negative test is requested.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Specimen collected with a nasal swab.
  • Negative samples from specimens confirmed SARS-CoV-2 negative by the gold standard, or positive samples from specimens confirmed SARS-CoV-2 positive by the gold standard.

排除标准

  • Specimens that have been stored at 4ºC for more than 24h
  • Specimens stored at -70ºC that have been under more than 2 freeze/thaw cycles
  • Specimens that have been stored at -20 for more than 10 days
  • Contamination and/or deterioration of the specimen that, in the investigator's opinion, may impact its handling and/or analysis

结局指标

主要结局

Sensitivity of the SARS-CoV-2 NAD Kit

时间窗: Immediately after the procedure

The investigators assessed the sensitivity as the capacity to correctly detect positive specimens of SARS-CoV-2 infection previously confirmed as positive (True Positive, TP) by the gold standard RT-PCR.

次要结局

  • Specificity of the SARS-CoV-2 NAD Kit(Immediately after the procedure)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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