Safety and efficacy of Ayush 64 tablets as an adjunct therapy and its effect on bio- markers in mild to moderate covid-19 patients

H. Nataraj, R. Suresh, Chennaveerappa, P. Rao, S. Shetty, S. Gopkrishna, S. Ambika, Padmanabha Lal
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Abstract

Background: COVID-19 has emerged as the latest pandemic that erupted in the Wuhan City of People’s Republic of China in December 2019, which is affecting human health and economy across the world. The ongoing COVID-19 outbreak in developed countries also highlights the fact that developed countries and rich populations are not immune to infectious disease outbreaks. Coronaviruses (CoVs) are enveloped, single-stranded, positive-sense RNA viruses that belong to the Coronaviridae family. SARS-CoV-2 is a member of the beta CoV genus, which also includes SARS-CoV-1 and MERS-CoV. The lack of approved effective drug therapeutic protocols for CoVs would make treating newly emerged COVID-19 infections globally difficult. Objective: A clinical study was conducted to evaluate the safety and efficacy of AYUSH 64 a poly herbal drug as an adjunct therapy to standard of care in mild to moderate Covid 19 patients Materials and methods: A prospective, open-label, randomized, parallel assignment, single-center clinical study with pre-test and post-test design was conducted at Covid hospital, Hassan institute of medical sciences between September 2020 to December 2020. A total 60 diagnosed cases (22-75 years of age) of Covid 19 were randomly allocated to both the groups. Control group received standard of care (SOC) as prescribed by the ICMR/WHO and state government, Trial Group received one week intervention of AYUSH 64 tablets at the dose of 2gm/day along with standard of care. Assessment of parameters viz. improvement in the symptoms, hematology, liver function, kidney function tests, acute phase reactants, Serum ferritin, Di dimer, LDH, and hsCRP were analyzed on day zero, day three and day seven. Results: One-week intervention of AYUSH-64 along with SOC helped to recover from Covid 19 symptoms. The intervention was safe on blood and biochemical parameters. Trial group has shown significant reduction in acute phase reactants viz hsCRP, LDH, Di dimer and Ferritin compare to the control group. No serious drug adverse effects were observed during the study. Conclusion: AYUSH-64 along-with standard care in mild to moderate covid 19 patients is safe and efficacious and this may be used as add-on to standard care for early recovery and better outcome.
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阿尤什64片辅助治疗轻、中度covid-19患者的安全性、有效性及其对生物标志物的影响
背景:2019冠状病毒病(COVID-19)是2019年12月在中华人民共和国武汉市爆发的最新一场大流行,正在影响全球人类健康和经济。目前在发达国家暴发的COVID-19疫情也凸显了一个事实,即发达国家和富裕人群并非对传染病暴发免疫。冠状病毒是一种包膜单链阳性RNA病毒,属于冠状病毒科。SARS-CoV-2是贝塔冠状病毒属的一员,贝塔冠状病毒属还包括SARS-CoV-1和MERS-CoV。缺乏经批准的有效的新冠病毒药物治疗方案将使全球新出现的COVID-19感染难以治疗。目的:开展临床研究,评价复方中草药AYUSH 64作为轻至中度新冠肺炎患者标准护理辅助治疗的安全性和有效性。材料和方法:2020年9月至2020年12月,在哈桑医学研究所新冠医院开展一项前瞻性、开放标签、随机、平行分配、单中心临床研究,采用前测试和后测试设计。将60例确诊病例(22-75岁)随机分为两组。对照组患者给予ICMR/WHO及邦政府规定的标准护理(SOC),试验组患者在给予标准护理的同时给予AYUSH 64片(2gm/d) 1周的干预。在第0天、第3天和第7天分析症状改善、血液学、肝功能、肾功能测试、急性期反应物、血清铁蛋白、二聚体、LDH和hsCRP等参数的评估。结果:AYUSH-64联合SOC干预1周有助于患者从新冠肺炎症状中恢复。干预对血液和生化指标是安全的。与对照组相比,试验组急性期反应物hsCRP、LDH、Di二聚体和铁蛋白明显减少。研究期间未观察到严重的药物不良反应。结论:AYUSH-64联合标准治疗在轻中度covid - 19患者中是安全有效的,可作为标准治疗的补充,用于早期康复和更好的结果。
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