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临床试验/CTRI/2020/05/025161
CTRI/2020/05/025161已完成2 期

A Randomized and Comparative Study to assess Safety and Efficacy of Supplemental Treatment of a herbal formulation - Aayudh Advance comprising essential oils in patients with Corona Virus 2019 (Covid-19)

Ms Shukla Ashar Impex Pvt Ltd0 个研究点目标入组 74 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
74

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1)Subject willing to sign informed consent.
  • 2)Subject age group of 18 years and above of both gender.
  • 3)All patients with COVID-19 RT-PCR positive (within 7 days)/ any Covid-19 test kit, admitted to the hospital / healthcare center will be eligible.
  • 4)Patients who are having mild to moderate symptoms of Covid-19 disease and tested positive for Covid-19 test.

排除标准

  • 1)Patient younger than18 years age.
  • 2)Women who are pregnant or who intend to become pregnant for the next three months after taking the drug.
  • 3)Patients allergic to type medications or any of the ingredient of the formulation.
  • 4)Patients with a neurological history (seizures, epilepsy, etc.).
  • 5)Patients with a previous history of psychiatric illnesses (depression, anxiety, suicide attempt).
  • 6)Patients with severe cardiac pathologies or relevant chronic diseases that in the judgment of the clinician recommend the non-inclusion of the patient in the study.
  • 7)Patients who are on artificial ventilation or oxygen supply.
  • 8)Very severe patients of Covid 19.
  • 9)Patients with severe hypertension, diabetes and other chronic diseases shall be excluded.

研究者

发起方
Ms Shukla Ashar Impex Pvt Ltd

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