CTRI/2020/06/025977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 120 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
- 120
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
- •Subject willing to sign informed consent.
- •Subject age group of 18 years and above of both gender.
- •All patients with COVID-19 PCR positive (within 7 days/high clinical suspicion admitted to Corona Virus study participating hospital will be eligible.
- •Patients who are having mild to moderate symptoms of Covid-19 disease and tested positive for Covid-19 test.
排除标准
- •Patients younger than 18 years.
- •Women who are pregnant or who intend to become pregnant for the next three months after taking the drug.
- •Patients allergic to type medications or any of the ingredient of the formulation.
- •Patients with a neurological history (seizures, epilepsy, etc.).
- •Patients with a previous history of psychiatric illnesses (depression, anxiety, suicide attempt).
- •Patients with cardiac pathologies or relevant chronic diseases that in the judgment of the clinician recommend the non-inclusion of the patient in the study.
- •Patients who would require artificial ventilation or oxygen supply.
- •Very severe patients of Covid 19.
- •Patients with severe hypertension, diabetes shall be excluded.
研究者
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