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临床试验/NCT02396355
NCT02396355已完成不适用

Accuracy Evaluation of the BD FACS Presto System: Instrument, Software and BD CD4/%CD4/Hb Cartridge Assay

Becton, Dickinson and Company6 个研究点 分布在 4 个国家目标入组 583 人开始时间: 2015年2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
583
试验地点
6
主要终点
Method bias between BD FACSPresto System vs. Predicate in venous blood (AbsCD4 and %CD4)

研究概览

简要总结

The enumeration of T lymphocytes positive for the CD4 antigen is used to determine the immune status of patients with, or suspected of developing, immune deficiencies such as AIDS. The BD FACS Presto™ is an investigational automated system for in vitro diagnostic use in performing the direct enumeration of CD4 absolute count, CD4 percentage of lymphocytes, and hemoglobin (Hb) concentration in human whole blood.

This is a prospective study to determine the relative bias between the investigational BD FACS Presto system and the predicate BD FACS Calibur with BD Tritest system in their determination of absolute CD4, % CD4, and Hb concentrations.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Subject has been infected with HIV and willing to provide informed consent to draw venous and capillary blood
  • Specimen: Venous blood must be collected in blood collection tube with EDTA anticoagulant and stored at room temperature (20-25 °C) according to tube manufacturer's instructions
  • Specimen: post enrolment staining within 24 hours
  • venous blood of acceptable quality for flow cytometry, e.g. no hemolysis or clots and acceptable pre analytical handling)
  • venous blood sample > 1 mL for sample preparation
  • capillary blood applied to the investigational CD4/%CD4/Hb cartridge

排除标准

  • Subject unwilling to disclose medical information regarding previous CD4 test results
  • Subject unwilling to discuss medical information regarding co-morbid conditions and current medications

结局指标

主要结局

Method bias between BD FACSPresto System vs. Predicate in venous blood (AbsCD4 and %CD4)

时间窗: assayed upon sample collection

The primary endpoint is the bias (expected difference) between the investigational vs. predicate system measured as absolute CD4 lymphocyte count and %CD4 in peripheral venous blood from a minimum of 400 specimens with valid results tested at three or more external sites.

次要结局

  • Method bias between BD FACSPresto System vs. Predicate in Capillary Blood (AbsCD4 and %CD4)(assayed upon sample collection)
  • Method bias between BD FACSPresto System vs. Predicate for Hemoglobin(assayed upon sample collection)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (6)

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