Effect of mulmina mango as an adjunct to standard of care treatment on COVID-19 positive subjects undergoing treatment for COVID-19 in hospital quarantine (Dedicated Covid Health Centre)

Ashwitha Shetty, M. Madhu, N. Rajesh, S. M. Ahmed
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Abstract

There are no approved drugs to treat COVID-19, and the vaccine is likely to be ready by early 2021. Many clinical studies are ongoing around the globe to find a cure or prevention of the disease. The objective of the proposed study is to determine the efficacy and safety profile of Mulmina Mango as an adjunct to standard of care treatment on COVID-19 positive subjects undergoing treatment for COVID-19 in Hospital Quarantine. Settings and Design: The enrolled subjects were randomized into either of the two treatment arms in the ratio of 1:1. The freshly diagnosed (24-48 hrs.) COVID-19 positive Male or Female is aged 20 to 65 years (both inclusive) hospitalized patients were approached and checked for their eligibility. They were recruited after signing the written informed consent form. The number of patients included in the study is 48. In efficacy, both the treatment arms and the reduction in clinical symptom scale value and ordinal scale value are seen on day 7. On the ordinal scale, 41.7% of subjects in Treatment arm A showed a reduction of 2 points on the day, and 16.7% of subjects show 2 points reduction in Treatment arm B. In Safety results, there was no clinically significant finding in safety parameters in Treatment arm B. Mulmina Mango showed encouraging results concerning RTPCR, CRP, Dopamine, IgG, CD4, and CD8 parameters. The properties of Mulmina Mango are highlighted below, along with the parameters for each property. Mulmina Mango, COVID-19, Treatment Arm A, Treatment Arm B, MoHFW (Ministry of Health and Family Welfare)
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莫米娜芒果辅助标准护理治疗对医院隔离治疗Covid -19阳性受试者的影响(专用Covid - Health Centre)
目前还没有批准的治疗COVID-19的药物,疫苗可能会在2021年初准备好。许多临床研究正在全球范围内进行,以寻找治疗或预防这种疾病的方法。拟议研究的目的是确定Mulmina Mango作为在医院隔离中接受COVID-19治疗的COVID-19阳性受试者的辅助标准护理治疗的有效性和安全性。设置和设计:入组受试者按1:1的比例随机分为两个治疗组。新诊断者(24-48小时)与年龄在20至65岁(含两种)的住院患者接触并检查其资格。他们在签署书面知情同意书后被招募。纳入研究的患者人数为48人。在疗效方面,治疗组和临床症状量表值和顺序量表值在第7天均有所下降。在顺序量表上,A组41.7%的受试者当天降低了2分,b组16.7%的受试者当天降低了2分。在安全性结果上,b组的安全性参数没有明显的临床意义。Mulmina Mango在RTPCR、CRP、多巴胺、IgG、CD4和CD8参数上显示出令人鼓舞的结果。下面突出显示了Mulmina Mango的属性,以及每个属性的参数。Mulmina Mango, COVID-19,治疗组A,治疗组B,卫生部(卫生和家庭福利部)
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