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题名

Chinese herbal medicine Shufeng Jiedu capsule for mild to moderate COVID-19: a multicenter, randomized, double-blind, placebo-controlled phase II trial

作者
通讯作者Liu, Jian-ping; Lu, Hong-zhou
发表日期
2024-05-27
DOI
发表期刊
EISSN
1663-9812
卷号15
摘要
Background: The COVID-19 pandemic has had a profound global impact, although the majority of recently infected cases have presented with mild to moderate symptoms. Previous clinical studies have demonstrated that Shufeng Jiedu (SFJD) capsule, a Chinese herbal patent medicine, effectively alleviates symptoms associated with the common cold, H1N1 influenza, and COVID-19. This study aimed to assess the efficacy and safety of SFJD capsules in managing symptoms of mild to moderate COVID-19 infection.Methods: A randomized, double-blind, placebo-controlled trial was conducted from May to December 2022 at two hospitals in China. Mild and moderate COVID-19-infected patients presenting respiratory symptoms within 3 days from onset were randomly assigned to either the SFJD or placebo groups in a 1:1 ratio. Individuals received SFJD capsules or a placebo three times daily for five consecutive days. Participants were followed up for more than 14 days after their RT-PCR nucleoid acid test for SARS-CoV-2 turned negative. The primary outcome measure was time to alleviate COVID-19 symptoms from baseline until the end of follow-up.Results: A total of 478 participants were screened; ultimately, 407 completed the trial after randomization (SFJD, n = 203; placebo, n = 204). No statistically significant difference in baseline parameters was observed between the two groups. The median time to alleviate all symptoms was 7 days in the SFJD group compared to 8 days in the placebo group (p = 0.037). Notably, the SFJD group significantly attenuated fever/chills (p = 0.04) and headache (p = 0.016) compared to the placebo group. Furthermore, the median time taken to reach normal body temperature within 24 h was reduced by 7 hours in the SFJD group compared to the placebo group (p = 0.033). No deaths or instances of serious or critical conditions occurred during this trial period; moreover, no serious adverse events were reported.Conclusion: The trial was conducted in a unique controlled hospital setting, and the 5-day treatment with SFJD capsules resulted in a 1-day reduction in overall symptoms, particularly headache and fever/chills, among COVID-19-infected participants with mild or moderate symptoms. Compared to placebo, SFJD capsules were found to be safe with fewer side effects. SFJD capsules could potentially serve as an effective treatment for alleviating mild to moderate symptoms of COVID-19.Clinical Trial Registration: https://www.isrctn.com/, identifier ISRCTN14236594.
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收录类别
语种
英语
学校署名
通讯
WOS研究方向
Pharmacology & Pharmacy
WOS类目
Pharmacology & Pharmacy
WOS记录号
WOS:001241282700001
出版者
来源库
Web of Science
引用统计
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/788153
专题南方科技大学第二附属医院
作者单位
1.Beijing Univ Chinese Med, Ctr Evidence Based Chinese Med, Beijing, Peoples R China
2.Southern Univ Sci & Technol, Peoples Hosp Shenzhen 3, Dept Dermatovenerol, Hosp Affiliated 2, Shenzhen, Guangdong, Peoples R China
3.Univ Med Ctr Hamburg Eppendorf, HanseMerkur Ctr Tradit Chinese Med, Hamburg, Germany
4.Peoples Hosp Bozhou, Bozhou, Peoples R China
5.Fudan Univ, Zhongshan Hosp Affiliated, Shanghai, Peoples R China
6.London South Bank Univ, Inst Hlth & Social Care, London, England
通讯作者单位南方科技大学第二附属医院
推荐引用方式
GB/T 7714
Lu, Chun-li,Yang, Liu-qing,Jin, Xin-yan,et al. Chinese herbal medicine Shufeng Jiedu capsule for mild to moderate COVID-19: a multicenter, randomized, double-blind, placebo-controlled phase II trial[J]. FRONTIERS IN PHARMACOLOGY,2024,15.
APA
Lu, Chun-li.,Yang, Liu-qing.,Jin, Xin-yan.,Friedemann, Thomas.,Li, Yu-fei.,...&Lu, Hong-zhou.(2024).Chinese herbal medicine Shufeng Jiedu capsule for mild to moderate COVID-19: a multicenter, randomized, double-blind, placebo-controlled phase II trial.FRONTIERS IN PHARMACOLOGY,15.
MLA
Lu, Chun-li,et al."Chinese herbal medicine Shufeng Jiedu capsule for mild to moderate COVID-19: a multicenter, randomized, double-blind, placebo-controlled phase II trial".FRONTIERS IN PHARMACOLOGY 15(2024).
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