Lu Chun-Li, Yang Liu-Qing, Jin Xin-Yan, Friedemann Thomas, Li Yu-Fei, Liu Xue-Han, Chen Xiao-Ying, Zou Xiang-Yun, Zhang Bing-Rui, Wang Fu-Xiang, Lin Yuan-Long, Tang Yi-Min, Cao Meng-Li, Jiang Ya-Lin, Gao You-Fang, Liu Kui, Tao Zhen-Gang, Robinson Nicola, Schröder Sven, Liu Jian-Ping, Lu Hong-Zhou
Centre for Evidence-Based Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
The Third People's Hospital of Shenzhen, The Second Affiliated Hospital to Southern University of Science and Technology, Shenzhen, China.
Front Pharmacol. 2024 May 27;15:1383831. doi: 10.3389/fphar.2024.1383831. eCollection 2024.
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. 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. A total of 478 participants were screened; ultimately, 407 completed the trial after randomization (SFJD, = 203; placebo, = 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 ( = 0.037). Notably, the SFJD group significantly attenuated fever/chills ( = 0.04) and headache ( = 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 ( = 0.033). No deaths or instances of serious or critical conditions occurred during this trial period; moreover, no serious adverse events were reported. 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. : https://www.isrctn.com/, identifier ISRCTN14236594.
新型冠状病毒肺炎疫情对全球产生了深远影响,尽管最近大多数感染病例表现为轻至中度症状。先前的临床研究表明,中药专利药疏风解毒胶囊能有效缓解普通感冒、甲型H1N1流感和新型冠状病毒肺炎相关症状。本研究旨在评估疏风解毒胶囊治疗轻至中度新型冠状病毒肺炎感染症状的疗效和安全性。2022年5月至12月在中国两家医院进行了一项随机、双盲、安慰剂对照试验。发病3天内出现呼吸道症状的轻至中度新型冠状病毒肺炎感染患者按1:1比例随机分为疏风解毒胶囊组或安慰剂组。个体连续5天每天服用3次疏风解毒胶囊或安慰剂。在严重急性呼吸综合征冠状病毒2逆转录聚合酶链反应核酸检测呈阴性后,对参与者进行了超过14天的随访。主要结局指标是从基线到随访结束缓解新型冠状病毒肺炎症状的时间。共筛查了478名参与者;最终,407名在随机分组后完成了试验(疏风解毒胶囊组,=203;安慰剂组,=204)。两组之间在基线参数上未观察到统计学显著差异。疏风解毒胶囊组缓解所有症状的中位时间为7天,而安慰剂组为8天(=0.037)。值得注意的是,与安慰剂组相比,疏风解毒胶囊组显著减轻了发热/寒战(=0.04)和头痛(=0.016)。此外,与安慰剂组相比,疏风解毒胶囊组在24小时内达到正常体温的中位时间缩短了7小时(=0.033)。在此试验期间未发生死亡或严重或危急情况;此外,未报告严重不良事件。该试验在独特的对照医院环境中进行,对于轻至中度症状的新型冠状病毒肺炎感染参与者,5天的疏风解毒胶囊治疗使总体症状减少了1天,尤其是头痛和发热/寒战。与安慰剂相比,发现疏风解毒胶囊安全且副作用较少。疏风解毒胶囊可能是缓解新型冠状病毒肺炎轻至中度症状的有效治疗方法。:https://www.isrctn.com/,标识符ISRCTN14236594 。