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. 2022 May 4;28(10):885–893. doi: 10.1007/s11655-022-3673-x

Effectiveness and Safety of Baidu Jieduan Granules for COVID-19: A Retrospective Observational Multicenter Study

Xiang-ru Xu 1, Wen Zhang 1, Xin-xin Wu 1, Ting-rong Huang 2, Jian-guo Zuo 3, Zhong Shao 4, Shuang Zhou 5, Bang-jiang Fang 1,6,
PMCID: PMC9068500  PMID: 35508863

Abstract

Objective

To evaluate the effectiveness and safety of Baidu Jieduan Granules (BDJDG) to treat common type coronavirus disease 2019 (COVID-19).

Methods

This multicenter, retrospective, and observational clinical trial included 230 common COVID-19 patients in Leishenshan, Huangshi, and Laohekou Hospitals in Wuhan from January 21 to March 26, 2020. The included patients were further divided into two subgroups according to the use of supplemental oxygen, mild and moderate groups. During the first 14 d of hospitalization, all patients were administered BDJDG combined with conventional Western medicine, and observed for continuous 28 d. Primary outcomes were disease progression rate and discharge rate. Secondary outcomes included negative conversion time of nucleic acid, hospitalization duration, clinical symptom subsidence time, and symptom regression rate.

Results

A total of 230 common COVID-19 patients were analyzed (138 in moderate group and 92 in mild group). By day 28, the disease progression rate was 4.3% and the discharge rate was 95.7%. All mild cases recovered and were discharged from hospital. The median negative conversion time of nucleic acid of all 230 COVID-19 patients was 12 d [inter-quartile range (IQR) 3.5–17], the median hospitalization duration was 15 d (IQR 12–20). The median time to fever, cough, and fatigue recovery was 4 d (IQR 2–6), 8 d (IQR 5–12), and 8 d (IQR 5–11). The recovery rate of fever, cough, and fatigue was 94.6%, 90.5%, and 93.5%. The median time to clinical improvement was 12 d (IQR 10–17). Compared with the baseline, total leukocyte counts, neutrophil counts, lymphocyte counts, and platelet counts were increased significantly on days 7 and 14 (P<0.01). C-reactive protein markedly increased on day 3 and significantly decreased on days 7 and 14 (P<0.01). No serious adverse events occurred during treatment.

Conclusion

BDJDG may be effective and safe for treatment of common type COVID-19. (Registration No. ChiCTR2000030836)

Electronic Supplementary Material

Supplementary material (Appendices 1—4) is available in the online version of this article at 10.1007/s11655-022-3673-x.

Keywords: COVID-19, common type, Baidu Jieduan Granule, integrated Chinese and Western medicine

Supplementary material

11655_2022_3673_MOESM1_ESM.pdf (206.6KB, pdf)

Effectiveness and Safety of Baidu Jieduan Granules for COVID-19: A Retrospective Observational Multicenter Study

Author Contributions

Funding acquisition and supervision: Fang BJ; investigation: Xu XR, Zhang W, Wu XX; methodology: Huang TR, Zuo JG, Shao Z; software: Xu XR; writing-original draft: Xu XR; writing—review & editing: Fang BJ, Shuang Z.

Footnotes

Supported by the National Key Research and Development Program Project (No. 2018YFC1705900), and the Emergency Committee of the World Federation of Chinese Medicine Societies and Shanghai Society of Traditional Chinese Medicine and Shanghai Society of Traditional Chinese Medicine, Novel Coronavirus Pneumonia Emergency Tackling Key Project (No. SJZLJZ.N01)

Conflict of Interest

The authors have no conflicts of interest to declare.

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Associated Data

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Supplementary Materials

11655_2022_3673_MOESM1_ESM.pdf (206.6KB, pdf)

Effectiveness and Safety of Baidu Jieduan Granules for COVID-19: A Retrospective Observational Multicenter Study


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