Clinical efficacy of Jingyin granules, a Chinese patent medicine, in treating patients infected with coronavirus disease 2019

被引:12
作者
Chen, Bowu [1 ]
Yu, Xiaoxiao [2 ]
Zhang, Lei [3 ]
Huang, Wenqi [4 ]
Lyu, Hua [5 ]
Xu, Yuping [6 ]
Shen, Jiaojiao [6 ]
Yuan, Weian [7 ]
Fang, Min [4 ]
Li, Man [2 ]
Gao, Yueqiu [1 ,2 ,8 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Dept Hepatopathy, Shanghai, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Lab Cellular Immun, Shanghai, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Gen Affairs Dept, Shanghai, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Adm Off, Shanghai, Peoples R China
[5] Natl Monitoring Ctr Med Serv Qual TCM Hosp, Shanghai, Peoples R China
[6] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Nursing Dept, Shanghai, Peoples R China
[7] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, GCP Ctr, Shanghai, Peoples R China
[8] Inst Infect Dis Integrated Tradit Chinese & Wester, Beijing, Peoples R China
关键词
SARS-CoV-2; Jingyin granules; Traditional Chinese medicine; Negative conversion rate; Negative conversion time; COVID-19;
D O I
10.1016/j.phymed.2022.154496
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Jingyin granules (JY), one patented Chinese herbal formula, have been advised for treating coronavirus disease 2019 (COVID-19) in China. As of now, the safety and effectiveness of JY in treating COVID-19 patients were still to be evaluated. Purpose: To investigate the safety and clinical effectiveness of JY in treating mild COVID-19 patients. Study design: We carried out a prospective cohort study, as the highly infectious COVID-19 omicron variant ranged in Shanghai (ClinicalTrial.gov registration number: ChiCTR2200058692). Methods: Participants infected with COVID-19, who were diagnosed as mild cases, were assigned to receive either JY (JY group) or traditional Chinese medicine placebo (placebo group) orally for 7 days. The primary clinical indicators were the RNA negative conversion rate (NCR) and the incidence of severe cases. The secondary clinical indicators were the negative conversion time (NCT), inpatient length of stay (ILOS), and the disappearance rates of clinical symptoms. Results: Nine hundred participants were recruited in this clinical trial study, and 830 patients met the eligibility criteria. Seven hundred and ninety-one patients, accomplished the following-up assessment, including 423 cases of JY group and 368 cases of placebo group. NCR in JY group at 7-day posttreatment was considerably greater compared with placebo group (89.8% [380/423] vs 82.6% [304/368], P = 0.003). None of the patients with mild COVID-19 developed into severe cases. The median NCT of SARS-CoV-2 and ILOS in JY group were lesser than that in placebo group (4.0 [3.0,6.0]vs 5.0 [4.0,7.0] days, P < 0.001; 6.0 [4.0, 8.0] vs 7.0 [5.0, 9.0] days, P < 0.001). In both groups, the obvious improvement in clinical symptoms was observed, but the difference was not significant. In the subgroup of age <= 60 years, JY promoted SARS-CoV-2 RNA negative conversion (HR=1.242; 95% CI: 1.069-1.444, P < 0.001). No patients in both groups were reported as the case of serious adverse event. Conclusion: JY maybe the potential medicine for treating mild COVID-19 patients, which had beneficial effects on increasing NCR, and shortening NCT and ILOS.
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页数:9
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