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临床试验/NCT01646411
NCT01646411Unknown不适用

Phase I Study for Positive IgM Antibody Detection in New Diagnostic Test Kit for for Acute Phase Infection

The Plasma Source1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
300
试验地点
1
主要终点
IgM greater than 1xcut off value

研究概览

简要总结

For the development of a Point of Care IVD test kit for acute phase disease detection against a variety of bacterial and viral infections. Phase one includes 100 clinical diagnosed positive and 200 clinically "normal" serum and whole blood matched specimens for specificity and sensitivity determination for each marker. The positive samples must be IgM positive using any FDA cleared ELISA test kit. The negatives samples must be negative for IgM.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • current acute infection
  • age 18-70
  • male or female
  • currently active symptoms

排除标准

  • 未提供

结局指标

主要结局

IgM greater than 1xcut off value

时间窗: Antibody value measured within seven days of specimen collection.

Elisa System positive results are greater than 1 times the cutoff. Negative less than 1x cutoff. Prevalence of IGM in general mid-atlantic population is less than 10% of study population.

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)

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