A Study to Evaluate the Performance, and Usability of TruPlex HIV/HepB/Syphilis Rapid Test
NCT:NCT07569913 · NOT_YET_RECRUITING
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NCT编号NCT07569913
状态NOT_YET_RECRUITING
开始日期2026-09-01
完成时间2027-06-01
简要摘要
To evaluate the clinical performance of each analyte (HIV, HBsAg, and Syphilis) on the TruPlex HIV/HepB/Syphilis Rapid Test (TruPlex Test) using capillary blood (fingerstick), EDTA whole blood, EDTA-plasma, and SST-serum samples collected by trained operators at point-of-care settings. Additionally, to evaluate the usability of the TruPlex test through: structured usability assessments, via a questionnaire, completed by trained operators in point-of-care settings.
官方来源
在 ClinicalTrials.gov 上查看 →数据来自 ClinicalTrials.gov API。有关最新状态,请参阅官方记录。