CTRI/2021/03/031616
进行中（未招募）
未知
Evaluating the Use of Flavour-Stimulated Oral Fluids Collection for Severe Acute Respiratory Syndrome Coronavirus 2 Detection by Reverse Transcriptase Polymerase Chain Reaction and Enzyme Linked Immunosorbent Assay - a Concordance Study.
Datar Cancer Genetics0 个研究点目标入组 0 人待定
概览
- 阶段
- 未知
- 干预措施
- 未指定
- 疾病 / 适应症
- Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
- 发起方
- Datar Cancer Genetics
- 状态
- 进行中（未招募）
- 最后更新
- 3年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •1\. Known COVID\-19 positive by RTPCR (with active infection)
- •Known COVID\-19 negative by RTPCR (tested within 7 days)
- •2\. Provision of Informed Consent
- •3\. Willing to provide Nasopharyngeal Swab as well as Buccal Cavity Swab
排除标准
- •1\. Pediatric patients.
- •2\. Inability to provide Informed Consent.
- •3\. Inability to provide Nasopharyngeal Swab and / or Buccal Cavity Swab.
- •4\. Other conditions: allergic to latex.
- •5\. Diagnosed with psychological conditions that restrict ability to comply with study procedures;
- •6\. Prisoners and pregnant women
- •7\. Subjects with pathologies relating to dental, oral and salivary conditions.
- •8\. Subjects with allergies related to the components used in the kit.
- •9\. Any other condition as judged by the PI which will restrict the ability to participate in the study and / or comply with study procedures.
结局指标
主要结局
未指定
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