Hareendran Nair, Rajani A Nayar, G. Sreekumar, Sheeja Chandran, SP Parvathy, KV ManeshKumar, Sreejith Satheesan, Shan Sasidharan
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All the patients were administered with ZingiVir-H tablet (500 mg) orally every 4th hour along with lukewarm water after light meal. The intervention was continued until the body temperature became normal. Body temperature, Complete Blood Count (CBC), Erythrocyte Sedimentation Rate (ESR), C-reactive protein (C-RP), Liver Function Test (LFT), and Renal Function Test (RFT) were recorded after treatment, first follow-up (on 7th day of discharge) and 2nd follow-up (on 30th day from first follow-up date). LFT and RFT were observed before treatment and 2nd follow-up (on 30th day from first follow-up date) and the results obtained were analyzed statistically. Repeated measurements with ANOVA recorded a significant decrease in body temperature (within an average of 4.3 days), CBC, ESR, C-RP after the intervention. The LFT and RFT parameters before and after treatments were within the recommended clinical range which established the hepato-renal safety of the ZingiVir-H in the study subjects. 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The intervention was continued until the body temperature became normal. Body temperature, Complete Blood Count (CBC), Erythrocyte Sedimentation Rate (ESR), C-reactive protein (C-RP), Liver Function Test (LFT), and Renal Function Test (RFT) were recorded after treatment, first follow-up (on 7th day of discharge) and 2nd follow-up (on 30th day from first follow-up date). LFT and RFT were observed before treatment and 2nd follow-up (on 30th day from first follow-up date) and the results obtained were analyzed statistically. Repeated measurements with ANOVA recorded a significant decrease in body temperature (within an average of 4.3 days), CBC, ESR, C-RP after the intervention. The LFT and RFT parameters before and after treatments were within the recommended clinical range which established the hepato-renal safety of the ZingiVir-H in the study subjects. This study proved that ZingiVir-H is highly effective and safe in managing viral fever (jwara). 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引用次数: 1
摘要
当生物体受到病原病毒的攻击,感染性病毒颗粒附着并进入易感细胞时,就会发生病毒感染。有几种抗病毒药物可用于治疗病毒感染。这项试点临床研究的目的是证明ZingiVir-H(一种草药阿育吠陀制剂)对确诊为病毒感染的住院成人的疗效和安全性的初步评估。从2019年10月3日至2019年12月28日,共有30名18岁以上出现发烧的患者被纳入试验前和试验后临床试验。所有患者每4小时口服一次ZingiVir-H片(500mg),并在餐后加温水。干预一直持续到体温恢复正常。记录治疗后、第一次随访(出院第7天)和第二次随访(第一次随访后第30天)的体温、全血细胞计数(CBC)、红细胞沉降率(ESR)、C反应蛋白(C-RP)、肝功能测试(LFT)和肾功能测试(RFT)。在治疗前和第二次随访(第一次随访后第30天)观察LFT和RFT,并对所得结果进行统计学分析。ANOVA重复测量记录了干预后体温(平均4.3天内)、CBC、ESR、C-RP的显著下降。治疗前后的LFT和RFT参数均在推荐的临床范围内,这确定了ZingiVir-H在研究受试者中的肝肾安全性。这项研究证明ZingiVir-H在治疗病毒性发热(jwara)方面是非常有效和安全的。引文:Nair HJ、Nayar RA、Sreekumar GS、Chandran S、Parvathy SP等人(2021)一项评估ZingiVir-H(HerboMineral药物)治疗病毒性发热患者安全性和有效性的试点临床研究。Curr Res Complement Altern Med 5:144。DOI:10.29011/22577-2201.100044 2第5卷;第01期Curr Res Complement Altern Med,开放获取期刊ISSN:2577-2201
A Pilot Clinical Study to Evaluate the Safety and Efficacy of ZingiVir-H, Herbo-Mineral Drug in Patients with Viral Fever
A viral infection develops when an organism’s body is attacked by pathogenic viruses, and infectious virus particles attach to and enter susceptible cells. There are a few antiviral medicines available to manage the viral infection. The objective of this pilot clinical study was to demonstrate the preliminary evaluation on the efficacy and safety of ZingiVir-H, a herbomineral Ayurvedic preparation in hospitalized adults diagnosed with viral infection. A total of thirty patients above 18 years of age presenting with fever were enrolled from 3rd October 2019 to 28th December 2019 for conducting the pre-test and post-test clinical trial. All the patients were administered with ZingiVir-H tablet (500 mg) orally every 4th hour along with lukewarm water after light meal. The intervention was continued until the body temperature became normal. Body temperature, Complete Blood Count (CBC), Erythrocyte Sedimentation Rate (ESR), C-reactive protein (C-RP), Liver Function Test (LFT), and Renal Function Test (RFT) were recorded after treatment, first follow-up (on 7th day of discharge) and 2nd follow-up (on 30th day from first follow-up date). LFT and RFT were observed before treatment and 2nd follow-up (on 30th day from first follow-up date) and the results obtained were analyzed statistically. Repeated measurements with ANOVA recorded a significant decrease in body temperature (within an average of 4.3 days), CBC, ESR, C-RP after the intervention. The LFT and RFT parameters before and after treatments were within the recommended clinical range which established the hepato-renal safety of the ZingiVir-H in the study subjects. This study proved that ZingiVir-H is highly effective and safe in managing viral fever (jwara). Citation: Nair HJ, Nayar RA, Sreekumar GS, Chandran S, Parvathy SP, et al. (2021) A Pilot Clinical Study to Evaluate the Safety and Efficacy of ZingiVir-H, HerboMineral Drug in Patients with Viral Fever. Curr Res Complement Altern Med 5: 144. DOI: 10.29011/2577-2201.100044 2 Volume 5; Issue 01 Curr Res Complement Altern Med, an open access journal ISSN: 2577-2201