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临床试验/NCT04920773
NCT04920773已完成不适用

Community-based Post-exposure Prophylaxis for COVID-19: Results and Implications of Ayurveda Practice Guidelines

NMP Medical Research Institute2 个研究点 分布在 1 个国家目标入组 216 人开始时间: 2021年5月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
216
试验地点
2
主要终点
Number of participants with active COVID-19

研究概览

简要总结

Specifically identified Ayurvedic preparations is recommended by ministry of AYUSH as post-exposure prophylaxis to efficaciously prevent a negative person who has come into contact with COVID-19-positive. Traditionally, recommended Ayurvedic preparations have been used as antioxidants, antimicrobial and anti-inflammatory properties. Particularly, Guduchi Ghanvati has been recognised with its ability to control viral attachment, viral replication and induce immune response in pre clinical settings, and found to be one among the most important drugs in Ayurveda to fight against COVID-19.

However, known gap in guideline implementation and its impact on preventing active infection in exposed cases is unclear. Study aimed to increase the use of recommended AYUSH guidelines by having registered AYUSH physicians provide these medications, when indicated, in community based participants after known exposure to the SARS-CoV-2 coronavirus.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Men or women 18 to 60 years of age
  • Household contact residing with the index case in the 14 days prior to index diagnosis within a residence without maintaining social distance
  • Access to device and internet for telephonic appointments and follow up

排除标准

  • Currently hospitalised
  • Symptomatic with fever, cough, or shortness of breath
  • Use of anti-malarial treatment or chemoprophylaxis
  • Moderately or Severely ill for any co-morbid condition requiring medical assistance.
  • Cognitive impairment

结局指标

主要结局

Number of participants with active COVID-19

时间窗: 14-days following exposure

PCR- proven COVID-19

次要结局

  • Time to symptoms onset(14-days)
  • Disease Severity(14 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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