Effect of an Ayurvedic Intervention (Ayush-64) as a Stand-Alone Treatment in Mild to Moderate COVID-19: An Exploratory Prospective Single-Arm Clinical Trial

Singh N R, Amit, Babita Yadav, Arun Gupta, Rakesh Rana, Vishakha Rajesh Wetal, Neha Dubey, Sophia Jameela, Richa Singhal, Shruti Khanduri, Sharma B S, Rao BCS, Bharti, Srikanth N, Dhiman K S
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引用次数: 1

Abstract

An Ayurvedic polyherbal formulation (Ayush-64) was repurposed for use in mild to moderate COVID-19 cases based on the supportive evidence obtained from a pilot study on its effect on Influenza like illness (ILI) and molecular docking study which revealed that several compounds isolated from Ayush-64 demonstrated antiviral activity. The study aims at evaluating the effect of an Ayurvedic intervention (Ayush-64) in mild to moderate COVID-19 patients. A prospective single arm, pilot study in mild to moderate COVID-19 patients.  The study was conducted at Chaudhary Brahm Prakash Ayurved Charak Sansthan (CBPACS), New Delhi, India. A total of 37 COVID-19 participants confirmed through RT-PCR were included in the study. The proportion of participants with negative SARS-CoV-2 on nasal or throat swab in a 2-day consecutive real-time RT-PCR test was evaluated as the secondary outcome. In the study, 86.1% of participants demonstrated clinical recovery with 14 days of use of Ayush-64 as stand-alone treatment without any other conventional medicines, out of which 75% clinically recovered within 8 days. Further, 69.4% of participants turned negative by the 15th day, out of which 50% became COVID-19 negative on the 8th day. No AE/ ADR was observed during the study. Ayush-64 may significantly facilitate clinical improvement in terms of duration for clinical recovery and attaining negative conversion in mild to moderate COVID-19 cases.
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阿育吠陀干预(Ayush-64)作为轻中度COVID-19单独治疗的效果:一项探索性前瞻性单组临床试验
基于一项关于其对流感样疾病(ILI)作用的初步研究和分子对接研究获得的支持性证据,一种阿育吠德多草药配方(Ayush-64)被重新用于治疗轻中度COVID-19病例,该研究显示,从Ayush-64中分离的几种化合物显示出抗病毒活性。该研究旨在评估阿育吠陀干预(Ayush-64)对轻中度COVID-19患者的影响。一项针对轻至中度COVID-19患者的前瞻性单组试点研究。这项研究是在印度新德里的Chaudhary Brahm Prakash Ayurved Charak Sansthan (CBPACS)进行的。共有37名通过RT-PCR确诊的COVID-19参与者被纳入研究。在连续2天的实时RT-PCR检测中,受试者鼻或咽拭子上SARS-CoV-2阴性的比例作为次要结局进行评估。在该研究中,86.1%的参与者在不使用任何其他常规药物的情况下,使用Ayush-64作为单独治疗14天后表现出临床恢复,其中75%的患者在8天内临床恢复。此外,69.4%的参与者在第15天变为阴性,其中50%的参与者在第8天变为阴性。研究过程中未发生不良反应。在轻至中度COVID-19病例中,Ayush-64可显著促进临床改善,缩短临床恢复时间并实现阴性转化。
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