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固本咳喘颗粒治疗慢性支气管炎的疗效及安全性:一项多中心随机对照试验

 

Authors Li D, Shang X, Hong E, Zhu H, Li C, Zhang Y, Du C, Liang Y, Zhang S, Sang H, Yang D, Zhang H

Received 11 April 2025

Accepted for publication 4 July 2025

Published 12 August 2025 Volume 2025:19 Pages 6885—6896

DOI https://doi.org/10.2147/DDDT.S528815

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Prof. Dr. Tin Wui Wong

Demin Li,1 Xiaofeng Shang,2 Er Hong,3 Hongyan Zhu,4 Chaopeng Li,5 Yiyuan Zhang,6 Chaoping Du,7 Yun Liang,8 Shuwei Zhang,9 Hongchao Sang,10 Daowen Yang,1 HongChun Zhang11 

1Department of Traditional Chinese Medicine for Pulmonary Diseases, Center of Respiratory Medicine, China-Japan Friendship Hospital, Beijing, 100029, People’s Republic of China; 2Department of Respiratory and Critical Care Medicine, Taiyuan Central Hospital, Taiyuan, 030009, People’s Republic of China; 3Department of Respiratory, Ningbo Municipal Hospital of Traditional Chinese Medicine, Affiliated to Zhejiang Chinese Medical University, Ningbo, 315010, People’s Republic of China; 4Department of Respiratory and Critical Care Medicine, The People’s Hospital of Xiangtan County, Xiangtan, Hunan, 315010, People’s Republic of China; 5Department of Cardiovascular Medicine, Xingtai City Xindu District People’s Hospital, Xintai, Hebei, 054001, People’s Republic of China; 6Department of Gastroenterology and Respiratory Medicine, People’s Hospital of Yanggu County, Liaocheng, Shandong, 252300, People’s Republic of China; 7Department of Respiratory, Xiyang Public Hospital, Jinzhong, Shanxi, 045399, People’s Republic of China; 8Department of Respiratory and Endocrinology, People’s Hospital of Sanyuan County, Xianyang, Shanxi, 713899, People’s Republic of China; 9Department of Respiratory, People’s Hospital of Mengyin County, Linyi, Shandong, 276299, People’s Republic of China; 10Longhua Hospital of Traditional Chinese Medicine, Chengde, Hebei, 068150, People’s Republic of China; 11Department of Traditional Chinese Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, Beijing, 100029, People’s Republic of China

Correspondence: HongChun Zhang, Department of Traditional Chinese Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, No. 2 Yinghua Garden East Street, Chaoyang District, Beijing, 100029, People’s Republic of China, Tel +86 13701226664, Email zhanghongchun_zryy@163.com

Background: Chronic bronchitis (CB) is an inflammatory respiratory disease characterized by high prevalence and treatment challenges. In recent years, the integration of traditional Chinese medicine (TCM) with conventional therapies has gained widespread application in CB management, showing promising clinical benefits.
Methods: This multicenter, randomized controlled trial, led by China-Japan Friendship Hospital in Beijing, China, enrolled 300 CB patients aged 18– 75 years. Participants were randomized (2:2:1) into three groups: Guben Kechuan Granules (experimental group, n=120), Guilong Kechuanning Capsules (positive drug control, n=120), and subject education (blank control, n=60). The treatment lasted 24 weeks, followed by a 24-week follow-up. Efficacy was assessed through symptom evaluation, acute exacerbation of CB (AECB) incidence, pulmonary function tests, immunological assessments, and quality of life measures. Safety was evaluated based on adverse event reporting. Data analysis was conducted using SAS 9.4 software.
Results: Of the enrolled patients, 299 participants (99.7%) completed the full analysis, 298 were included in the safety assessment, and 278 entered the per-protocol efficacy analysis. Compared to the blank control group, Guben Kechuan Granules significantly reduced the time to first AECB, as well as the duration, severity, and frequency of AECB episodes (all p< 0.05). After 24 weeks of treatment, symptom scores for cough (− 21.85± 19.73), expectoration (− 22.74± 18.66), and wheezing (− 21.33± 18.76) showed substantial improvement (p< 0.05). These benefits persisted throughout the 24-week follow-up (p< 0.05). Additionally, significant improvements were observed in mobility, self-care, daily activities, and overall health status in the experimental group (all p< 0.05). However, no significant changes were observed in lung function parameters—including FEV1/FVC%, FEV1%pred, PEF, MMEF, FVC, or FEV1—across all three groups after 24 weeks of treatment. No serious adverse events were reported in the experimental group during follow-up.
Conclusion: Guben Kechuan Granules demonstrated significant efficacy and safety in CB management, alleviating clinical symptoms, reducing AECB incidence and severity, and enhancing patients’ quality of life.
Trial Registration: This trial is registered on 4 September 2022. Registration number: ChiCTR2200063321. Source(s) of funding: Traditional Chinese Medicine Inheritance and Innovation “Ten-Hundred-Thousand” Talents Program (Qihuang Program, grant number:2019-QTL-003). Chinese Clinical Trials Registry: https://www.chictr.org.cn/showproj.html?proj=177683.

Keywords: Guben Kechuan Granules, chronic bronchitis, efficacy, safety, randomized controlled trial