跳至主要内容
临床试验/CTRI/2021/01/030661
CTRI/2021/01/030661尚未招募未知

Pilot study of Svasth Viral Detection Device in detecting Covid-19 patients and viral load in patients in comparison with RT-PCR. - SVASTH viral scan

Miisky Technovation Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1 Age 25-80 years (both inclusive) at the time of signing ICF
  • 2 Patients who have tested positive for RT-PCR testing & are undergoing treatment as inpatients
  • 3 Voluntarily participating in the clinical study fully understanding and being fully informed of the study and having signed the Informed Consent Form (ICF); willingness and capability to complete all the study procedures
  • 4 Patients who have tested negative for RT-PCR testing either for initial detection or post Covi-19 treatment

排除标准

  • 1 Participation in this study will not be in the best interest of the subject, or any other circumstances that prevent the subject from participating in the study safely
  • 2 Cross reactive viral positive for HIV, HbsAg, NL-63, CoV1.
  • 3 Pregnant & Lactating women.

研究者

发起方
Miisky Technovation Pvt Ltd

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