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Chinese Medicine Formula Huashibaidu Granule Early Treatment for Mild COVID-19 Patients: An Unblinded, Cluster-Randomized Clinical Trial

Authors :
Chen Zhao
Li Li
Wei Yang
Wenliang Lv
Jian Wang
Jing Guo
Yu Dong
Nannan Shi
Cheng Lu
Zhiqiang Li
Zhan Shi
Renbo Chen
Ruili Huo
Qianzi Che
Yaxin Tian
Xinghua Xiang
Junhui Zhou
Yongjun Bian
Suping Chen
Yang Chen
Yingying Chen
Xiaodong Cong
Guoju Dong
Lijie Hu
Jianxin Jiang
Luxing Leng
Bin Li
Dongxu Li
Hao Li
Jing Li
Wensheng Qi
Qing Miao
Huaxin Shi
Jiaheng Shi
Bing Wang
Gang Wang
Wei Wang
Yongyue Xian
Xiaolei Xie
Chunyan Xu
Ming Xu
Bei Yan
Jinliang Yang
Li Zhang
Zhenqi Zhou
Haoning Zhu
Yibai Xiong
Bin Liu
Luqi Huang
Source :
Frontiers in Medicine, Vol 8 (2021)
Publication Year :
2021
Publisher :
Frontiers Media S.A., 2021.

Abstract

Background: Previous research suggested that Chinese Medicine (CM) Formula Huashibaidu granule might shorten the disease course in coronavirus disease 2019 (COVID-19) patients. This research aimed to investigate the early treatment effect of Huashibaidu granule in well-managed patients with mild COVID-19.Methods: An unblinded cluster-randomized clinical trial was conducted at the Dongxihu FangCang hospital. Two cabins were randomly allocated to a CM or control group, with 204 mild COVID-19 participants in each cabin. All participants received conventional treatment over a 7 day period, while the ones in CM group were additionally given Huashibaidu granule 10 g twice daily. Participants were followed up to their clinical endpoint. The primary outcome was worsening symptoms before the clinical endpoint. The secondary outcomes were cure and discharge before the clinical endpoint and alleviation of composite symptoms after the 7 days of treatment.Results: All 408 participants were followed up to their clinical endpoint and included in statistical analysis. Baseline characteristics were comparable between the two groups (P > 0.05). The number of worsening patients in the CM group was 5 (2.5%), and that in the control group was 16 (7.8%) with a significant difference between groups (P = 0.014). Eight foreseeable mild adverse events occurred without statistical difference between groups (P = 0.151).Conclusion: Seven days of early treatment with Huashibaidu granule reduced the likelihood of worsening symptoms in patients with mild COVID-19. Our study supports Huashibaidu granule as an active option for early treatment of mild COVID-19 in similar well-managed medical environments.Clinical Trial Registration:www.chictr.org.cn/showproj.aspx?proj=49408, identifier: ChiCTR2000029763.

Details

Language :
English
ISSN :
2296858X
Volume :
8
Database :
Directory of Open Access Journals
Journal :
Frontiers in Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.755338dbb672463db78f409d987d1fc6
Document Type :
article
Full Text :
https://doi.org/10.3389/fmed.2021.696976