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临床试验/NCT00951795
NCT00951795撤回不适用

Clinical Evaluation of the Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts

Abbott RDx Cardiometabolic3 个研究点 分布在 1 个国家开始时间: 2009年9月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
3

研究概览

简要总结

This is a multi-center study designed to assess the accuracy of Pima™ CD4 Test to enumerate CD4+ T-cells in whole blood over the measurement range expected for the intended population. The Pima CD4 Test consists of the Pima™ CD4 cartridge and Pima™ Analyzer to identify and determine the absolute counts of mature helper (CD3+/CD4+) T-lymphocytes in whole blood.

详细描述

Blood samples will be collected from HIV infected adolescents and adult men and women presenting to a physician's office or outpatient clinic. Capillary whole blood samples will be obtained by fingerstick in duplicate from all Subjects in the study for immediate measurement of CD4+ T-cell count on the Pima CD4 Test by a trained healthcare professional. Venous whole blood samples from all Subjects in the study will also be collected and transported to the clinical laboratory of each study site for concurrent testing on the reference method by a trained laboratory professional. Venous samples from all Subjects in the study will also be measured on the Pima CD4 Test at the study site. Hematocrit will also be measured for all Subjects.

研究设计

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

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 12 years of age or older
  • Confirmed HIV infection, HIV-1 or HIV-2 according to medical history (this inclusion will be waived for healthy non-HIV infected individuals who may need to be enrolled in order to fill the high end of the CD4+ T-cell measurement range of the Pima CD4 Test.
  • Subject agrees to complete all aspects of the study

排除标准

  • Subject has already participated in this study at a previous date
  • Subject is enrolled in a study to evaluate a new drug
  • Patient unable or unwilling to provide informed consent
  • Vulnerable populations as deemed inappropriate for study by site principal investigator.

研究者

发起方
Abbott RDx Cardiometabolic
申办方类型
Other

研究点 (3)

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