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金花清感颗粒联合西药治疗新型冠状病毒肺炎确诊及疑似病例的疗效:一项随机对照试验

Efficacy of Jinhua Qinggan Granules Combined With Western Medicine in the Treatment of Confirmed and Suspected COVID-19: A Randomized Controlled Trial.

作者信息

An XueDong, Xu Xi, Xiao MingZhong, Min XiaoJun, Lyu Yi, Tian JiaXing, Ke Jia, Lang SuPing, Zhang Qing, Fan An, Liu BinBin, Zhang Ying, Hu YaLing, Zhou YaNa, Shao JiaKai, Li XiaoDong, Lian FengMei, Tong XiaoLin

机构信息

Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan, China.

出版信息

Front Med (Lausanne). 2021 Oct 12;8:728055. doi: 10.3389/fmed.2021.728055. eCollection 2021.

Abstract

To conduct a randomized controlled clinical trial to evaluate the clinical efficacy and prognostic value of Jinhua Qinggan granules in patients with confirmed and suspected coronavirus disease 2019 (COVID-19). A total of 123 suspected and confirmed COVID-19 patients participated in this clinical trial and were randomly divided into Jinhua and Western medicine groups. For 14 days, the Jinhua group was treated with Jinhua Qinggan granules and antiviral drugs, and the Western medicine group was treated with antiviral drugs alone. We collected information on clinical symptoms, disease aggravation rates, and negative conversion rates of nucleic acids in patients, and observed the effects of anti-infective drugs. There was no significant difference in symptom improvement rates between the two groups, both confirmed and suspected patients ( > 0.05). Both treatments relieved symptoms such as fever, fatigue, and diarrhea. However, the Jinhua treatment was superior in relieving fever and poor appetite. Anti-infective drug use rates were significantly lower in the Jinhua group than in the control group. Jinhua Qinggan granules combined with Western medicine could relieve the clinical symptoms of fever and poor appetite in COVID-19 patients, reduce the use of antibiotics to a certain extent. The registration number at China Clinical Trial Registry is ChiCTR2000029601.

摘要

开展一项随机对照临床试验,以评估金花清感颗粒对确诊及疑似新型冠状病毒肺炎(COVID-19)患者的临床疗效和预后价值。共有123例疑似和确诊的COVID-19患者参与了这项临床试验,并被随机分为金花组和西药组。为期14天,金花组接受金花清感颗粒和抗病毒药物治疗,西药组仅接受抗病毒药物治疗。我们收集了患者的临床症状、疾病加重率和核酸转阴率等信息,并观察了抗感染药物的效果。两组(确诊和疑似患者)的症状改善率无显著差异(>0.05)。两种治疗方法均缓解了发热、乏力和腹泻等症状。然而,金花组在缓解发热和食欲不振方面更具优势。金花组的抗感染药物使用率显著低于对照组。金花清感颗粒联合西药可缓解COVID-19患者发热和食欲不振的临床症状,在一定程度上减少抗生素的使用。中国临床试验注册中心注册号为ChiCTR2000029601。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f3d/8545827/3297fe22a96c/fmed-08-728055-g0001.jpg

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