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A randomized clinical study to evaluate the efficacy and safety of OUTBREAK in mild and moderate COVID19 positive patients 一项评估疫情在covid - 19轻中度阳性患者中的有效性和安全性的随机临床研究
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.02.001
C. Suriyan, J. Martina, T. Sathishkumar, R. Ramesh, G. Prasannaraj
To evaluate the efficacy and safety of synthesized drug OUTBREAK, an Ayurvedic formulation for fever of viral origin in mild and moderate COVID19 positive patients. This is the prospective, randomized, multicentre, open label, parallel group interventional clinical endpoint study. Patients coming for the general outpatient department, were screened for viral fever by using the hematological, Biochemical and microbiological antibody assays. One Hundred patients who satisfied the selection criteria were enrolled in the study. Participants were randomized into 2 groups with 50 patients in each group. Patients were given standard treatment. In addition, Tab. OUTBREAK of Bageo Pharmaceuticals Pvt. Ltd., was administered to test groups. There is a highly significant improvement (P<0.001) in the subjects temperature, fever score, headache and SpO2 suggesting a good Analgesic and antipyretic activity of OUTBREAK. There is asignificant improvement in platelet count in the OUTBREAK treated group (P<0.01) when compared to the control group, proving its efficacy intreating thrombocytopenia. The improvement (P<0.01) in the random Sugar level in the OUTBREAK treated group depicts the anti-diabetic property of OUTBREAK.The improvement (P<0.01) in the WBC count in the OUTBREAK treated group depicts the antiviral property of OUTBREAK. The overall quality of life was better in OUTBREAK treated group compared to the control group. There were no serious adverse events reported. OUTBREAK is safe and efficacious in reversing thrombocytopenia and thus normalizing the platelet counts and relieving the clinical signs and symptoms (fever, headache and SpO2) of viral fever associated with thrombocytopenia and other cases of viral fever without thrombocytopenia. OUTBREAK is having good anti-viral, anti-pyretic and immuno-modulatory property.
评价阿育吠德复方药物OUTBREAK治疗新冠肺炎轻、中度阳性患者病毒性发热的疗效和安全性。这是一项前瞻性、随机、多中心、开放标签、平行组的干预性临床终点研究。通过血液学、生化和微生物抗体检测来筛查普通门诊患者是否有病毒性发热。100名符合选择标准的患者被纳入研究。参与者随机分为两组,每组50例。患者接受标准治疗。此外,Tab。对实验组进行了Bageo制药有限公司爆发的治疗。患者的体温、发热评分、头痛和SpO2均有显著改善(P<0.001),提示患儿具有良好的镇痛和解热作用。与对照组相比,治疗组血小板计数有显著改善(P<0.01),证明其治疗血小板减少症的疗效。治疗组随机糖水平的改善(P<0.01)反映了OUTBREAK的抗糖尿病特性。治疗组WBC计数的改善(P<0.01)说明了OUTBREAK的抗病毒特性。治疗组总体生活质量优于对照组。没有严重的不良事件报告。暴发在逆转血小板减少方面是安全有效的,从而使血小板计数正常化,并缓解伴有血小板减少的病毒性发热和其他无血小板减少的病毒性发热病例的临床体征和症状(发热、头痛和SpO2)。该菌具有良好的抗病毒、解热和免疫调节作用。
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引用次数: 0
Antidiabetic Activity Of Selenicereus Undatus (Haw). Fruit Extract Against Alloxan Induced Diabetic Mice 亚硒酸盐的抗糖尿病活性。水果提取物抗四氧嘧啶诱导的糖尿病小鼠
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.005
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引用次数: 0
Evaluation of the lethality of fractional extracts of Artemisia vulgaris on the Artemia salina larvae. 寻常蒿提取物对盐渍蒿幼虫的致死性评价。
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.02.002
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引用次数: 0
Antidiabetic activity of alcoholic extract of Momordica charantia and Murraya koenigii in alloxan induced albino rat 四氧嘧啶诱导的白化大鼠苦瓜和木鳖醇提物的抗糖尿病活性
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.014
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引用次数: 0
Mechanistic Approach Of Topoisomerase Ii ? Inhibitors For Anticancer Activity: A Review 拓扑异构酶Ii的机制研究抗癌活性抑制剂:综述
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.02.003
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引用次数: 0
Uv-Spectrophotomeric Method Development And Validation Of Synthesized Benzimidazole Derivative. 紫外分光光度法合成苯并咪唑衍生物的建立与验证。
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.009
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引用次数: 0
The Effect of Bergenia ligulata WALL in prediabetes: A randomized single-blind placebo-controlled study. 舌根草在糖尿病前期的作用:一项随机单盲安慰剂对照研究。
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.024
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引用次数: 0
Urtica dioica L.: A Review of its Nutritional and Pharmacological Activities 枸杞的营养和药理活性研究进展
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.004
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引用次数: 1
The Effect of Green Tea Leaves (Camellia Sinensis) Ethanol Extract Administration on The Ephitelium Thickness of Seminiferous Tubules and Number of Sertoli Cell in Mice (Mus Musculus) Exposed to 2,3,7,8-Tetrachlorodibenzo-P-Dioxin (TCDD) 绿茶(Camellia Sinensis)乙醇提取物对2,3,7,8-四氯二苯并-对二恶英(TCDD)暴露小鼠精小管上皮厚度和支持细胞数量的影响
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.001
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引用次数: 0
A comparative study to evaluate the use of saline nasal lavage and gargling in patients with Covid-19 infection. 生理盐水洗鼻与漱口在Covid-19感染患者中的应用对比研究
Pub Date : 2022-01-01 DOI: 10.31838/ijpr/2022.14.01.003
R. Jadhav, S. Patil, P. Deolekar, Pamelle Yadav, K. Dongerkery
Introduction: The infection caused by COVID-19 ranges from mild to moderate infection, but it can also cause severe infection and death in some people mostly in people who are old, or immunocompromisedSARS-CoV-2 has shown evidence of having higher capacity of binding to human cells and can settle in upper and lower portion of the respiratory tract it being the two important hotspots. Symptoms localized to the upper respiratory tract are mild which usually includes anosmia/hyposmia, ageusia/ dysgeusia, rhinitis along with sore throat. Material and methods: This study included individuals who were diagnosed with COVID-19 having mild symptoms of the disease which could be managed at their homes.Random assignment (50/50 chance) of subjects was done into two groups (A and B) for this study. Participants in group A were asked to perform the nasal washing and gargling with salt water up to 10 times a day for 14 days or until they felt better.Results:The leading cause for hospitalization for 15 (53.57%) people was that the oxygen saturation fell to below 93. Some scores compared between the two groups showed significant results in parameters of headache, postnasal drip, anosmia, sinusitis, sore throat, body ache, dry cough by unpaired two tailed P test. The age groups of 26 to 35, and 56 to 65 had comparatively higher values of adherence as compared to different age groups.Conclusion:The study demonstrates the hypothesis that nasal irrigation and saline gargling can have promising results to reduce the severity of COVID-19 infection when initiated within 24 hours of a positive test.
COVID-19引起的感染范围从轻度到中度感染,但也可导致一些人严重感染和死亡,主要发生在老年人或免疫功能低下的人群中。有证据表明,sars - cov -2具有更高的与人体细胞结合的能力,可以在上呼吸道和下呼吸道定居,这是两个重要的热点。局限于上呼吸道的症状是轻微的,通常包括嗅觉缺失/嗅觉减退、听觉障碍/听觉障碍、鼻炎和喉咙痛。材料和方法:本研究包括被诊断患有COVID-19且症状轻微的个体,这些个体可以在家中进行治疗。本研究将受试者随机分配(50/50的机会)分为两组(A组和B组)。A组的参与者被要求每天用盐水洗鼻和漱口10次,持续14天,或者直到他们感觉好些为止。结果:15人(53.57%)因血氧饱和度低于93而住院。两组患者在头痛、鼻后滴涕、嗅觉丧失、鼻窦炎、咽痛、体痛、干咳等指标上的非配对双尾P检验均有显著性差异。26 ~ 35岁和56 ~ 65岁年龄组的依从性相对较高。结论:本研究证实了一个假设,即在检测呈阳性的24小时内进行鼻腔冲洗和生理盐水漱口可以降低COVID-19感染的严重程度。
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引用次数: 3
期刊
International Journal of Pharmaceutical Research
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