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临床试验/NCT01488721
NCT01488721已完成不适用

Clinical Evaluation of the xMAP® NeoPlex4™ Assay for Detection of T4, TSH, 17-OHP and IRT Using the NeoPlex System

Luminex Corporation3 个研究点 分布在 1 个国家目标入组 7,462 人开始时间: 2011年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
7,462
试验地点
3

研究概览

简要总结

The purpose of this study is to assess the agreement of clinical performance between the proposed NeoPlex 4 assay and NeoPlex System and the comparator devices in clinical use in newborn screening programs for detection of T4, TSH, 17-OHP and IRT.

详细描述

The proposed (investigational) NeoPlex4 assay measures levels of thyroxine (T4), thyrotropin (hTSH), 17-alpha-OH-progesterone (17-OHP) and immunoreactive trypsinogen (IRT) from dried blood specimens (DBS) collected from neonates to screen for congenital hypothyroidism (CH), congenital adrenal hyperplasia (CAH) and cystic fibrosis (CF). The Clinical Evaluation of the xMAP® NeoPlex4™ Assay (NeoPlex4) for Detection of T4, TSH, 17-OHP and IRT using the NeoPlex System is a multi-center method concordance study on a combination of prospectively collected neonatal dried blood spots and pre-selected archived frozen dried blood spots that have been demonstrated to be positive for 17-OHP (CAH), IRT (CF), and T4 or TSH (CH). The study will be conducted at selected sites that routinely perform newborn screening testing in the United States.

研究设计

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

入排标准

年龄范围
1 Day 至 7 Days(Child)
性别
All
接受健康志愿者

入选标准

  • The dried blood spot specimen was collected on an FDA-cleared collection paper that has not yet passed its expiration dating.
  • Prospective specimens used in this study should only be those collected for the first time from a subject, or initial collection specimens.

排除标准

  • Collected within 24 hours of birth.
  • Specimens stored at ambient temperature for greater than 14 days prior to testing.
  • The specimen DBS appears diluted.
  • The specimen DBS shows evidence of clotting, caking, layering or serum rings.
  • The DBS punched disks were punched too close to the edge of the blood spot or show printed markings.
  • The specimen or collection card was contaminated with fecal material.
  • Non-eluting blood spot due to deterioration of sample caused by exposure to heat and humidity.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (3)

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