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临床试验/NCT03796546
NCT03796546已完成不适用

A Prospective Trial to Investigate the Clinical Utility and Application of a Next Generation Sequencing Test for Pathogen Detection of Cerebral Spinal Fluid (CSF) Samples to Diagnose Pediatric Central Nervous System (CNS) Infections

IDbyDNA, Inc.3 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2019年1月22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
IDbyDNA, Inc.
入组人数
71
试验地点
3
主要终点
Diagnostic Rate

研究概览

简要总结

Prospective, multi-site, study to evaluate the diagnosis rate of DNA and RNA sequencing of cerebrospinal fluid for identification of pathogens directly in patients who have already had a spinal tap to evaluate for infection and were found to have a pleocytosis. Diagnostic rate and clinical utility of concurrent standard testing will be compared to diagnostic rate and clinical utility of DNA and RNA sequencing.

详细描述

IDbyDNA, Inc. has developed a robust sequencing reference database for viruses, bacteria, fungi and parasites and developed novel analysis methods to analyze next-generation (NGS) sequencing data to rapidly identify infectious agents. This technology suite, known as the Explify™ platform, holds the promise to improve patient care and efficiently guide provider treatment planning for those suffering from infectious disease.

The PIPSEC trial, developed by pediatric physicians specializing in genomic medicine, is intended to facilitate the acquisition of high quality and clinically annotated biospecimens for the purpose of research discovery. This project intends to advance metagenomics, microbial genetics, bioinformatics and data analytics, for pathogen detection utilizing cerebral spinal fluid (CSF) specimens to contribute to the diagnosis of infectious agents impacting the central nervous system among pediatric patients. Clinically annotated specimens will facilitate continued development and validation of the Explify test and its clinical utility for providers treating central nervous system (CNS) infections.

The primary objective is to assess clinical utility of the Explify test compared to concurrent standard of care testing to identify pathogens from CSF fluid within a pediatric patient population.

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
0 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age 0-17 years of age (not yet 18)
  • Clinical evaluation for CNS infection
  • CSF white blood cell count (WBC) > 15 cells/µL when there are less than 5000 RBCs on same
  • Admitted to a participating study site
  • CSF obtained per standard protocol
  • 1 mL of appropriately stored CSF is available following completion of all standard of care testing

排除标准

  • CSF Red blood cell (RBC) count > 5000 cells/µL on same CSF sample as with pleocytosis
  • Unable to obtain consent

结局指标

主要结局

Diagnostic Rate

时间窗: 24 months

Comparison of the sensitivity, specificity, positive and negative predictive values of IDbyDNA NGS results with the Explify diagnostic platform compared with standard care.

次要结局

  • Clinical Utilization(24 months)

研究者

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

研究点 (3)

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