BPG is committed to discovery and dissemination of knowledge
Clinical Trials Study
Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Diabetes. Mar 15, 2026; 17(3): 114002
Published online Mar 15, 2026. doi: 10.4239/wjd.v17.i3.114002
Compound danshen dripping pills for diabetic retinopathy in patients with type 2 diabetes: A superiority, randomized controlled trial
Xue-Dong An, Guo-Liang Zhang, Yue-Hong Zhang, De Jin, Hang-Yu Ji, Li-Juan Wei, Ya-Lin He, Yan-Lin Zheng, Du-Jun Li, Xing-Wei Wu, Yuan-Bin Li, Jian Zhou, Shao-Jian Tan, Ming-Chang Zhang, Ke Fan, Shan Lu, Jing-Sheng Yu, Yu-Liang Wang, Shao-Jun Chen, Qiu-Hong Liu, Ming Jin, Lie Wu, Feng-Mei Lian, Xiao-Lin Tong
Xue-Dong An, Feng-Mei Lian, Department of Endocrinology, Guang’anmen Hospital, Beijing 100053, China
Guo-Liang Zhang, Lie Wu, Department of Ophthalmology, Guang'anmen Hospital, Chinese Academy of Traditional Chinese Medicine, Beijing 100053, China
Yue-Hong Zhang, Department of Endocrinology, Fangshan Hospital of Beijing University of Chinese Medicine, Beijing 102400, China
De Jin, Department of Nephrology, Hangzhou Traditional Chinese Medicine Hospital, Hangzhou 310007, Zhejiang Province, China
Hang-Yu Ji, Department of Gastroenterology, Guang’anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China
Li-Juan Wei, Department of Ophthalmology, The Affiliated Hospital of Changchun University of Chinese Medicine, Changchun 130012, Jilin Province, China
Ya-Lin He, Department of Ophthalmology, Jiangxi Provincial People's Hospital, Nanchang 338025, Jiangxi Province, China
Yan-Lin Zheng, Department of Ophthalmology, Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu 610075, Sichuan Province, China
Du-Jun Li, Department of Ophthalmology, Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan 434001, Hubei Province, China
Xing-Wei Wu, Department of Ophthalmology, Shanghai First People's Hospital, Shanghai 200080, China
Yuan-Bin Li, Department of Ophthalmology, Yantai Yuhuangding Hospital, Yantai 264000, Shandong Province, China
Jian Zhou, Department of Ophthalmology, Oriental Hospital, Beijing University of Chinese Medicine, Beijing 100078, China
Shao-Jian Tan, Department of Ophthalmology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
Ming-Chang Zhang, Department of Ophthalmology, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China
Ke Fan, Department of Ophthalmology, Henan Provincial Eye Center, Zhengzhou 450044, Henan Province, China
Shan Lu, Department of Ophthalmology, Shenyang He's Eye Hospital, Shengyang 110000, Liaoning Province, China
Jing-Sheng Yu, Department of Ophthalmology, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha 410007, Hunan Province, China
Yu-Liang Wang, Department of Ophthalmology, Jiangsu Provincial Hospital of Traditional Chinese Medicine, Nanjing 210029, Jiangsu Province, China
Shao-Jun Chen, Department of Ophthalmology, The First Affiliated Hospital of the Third Military Medical University of the People's Liberation Army, Chongqing 400038, China
Qiu-Hong Liu, Department of Ophthalmology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510405, Guangdong Province, China
Ming Jin, Department of Ophthalmology, China-Japan Friendship Hospital, Beijing 100029, China
Xiao-Lin Tong, Metabolic Disease Research Institute, Guang’anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China
Co-first authors: Xue-Dong An and Guo-Liang Zhang.
Co-corresponding authors: Feng-Mei Lian and Xiao-Lin Tong.
Author contributions: An XD, Zhang YH, Jin D, Ji HY and Zhang GL drafted the manuscript; Wu L, Lian FM and Tong XL designed this study and revised the manuscript; Zhang GL, Lian FM, Wu L, Tong XL, Zhou J, Jin M, Fan K; He YL, Li DJ, Zhang MC, Yu JS, Wu XW, Li YB, Wang YL, Wei LJ, Lu S, Liu QH, Zheng YL, Chen SJ, Tan SJ performed the clinical study, reviewed the draft and approved the final manuscript; Lian FM and Tong XL have played important and indispensable roles in the manuscript preparation as the co-corresponding authors.
Supported by The Science and Technology Innovation Project of Chinese Academy of Traditional Chinese Medicine, No. CI2021A02610; and the State Key Laboratory of Core Technology in Innovative Chinese Medicine, along with the Innovation Team and Talents Cultivation Program of the National Administration of Traditional Chinese Medicine, No. ZYYCXTD-D-202001.
Institutional review board statement: The study was approved by the Ethics Committee of Guang’anmen Hospital of the China Academy of Chinese Medical Sciences (Approval number: 2013EC059-01). Participants diagnosed with NPDR were recruited in 16 centers (Supplementary material).
Clinical trial registration statement: Phase III Study of Compound Danshen Dripping Pills to Treat Diabetic Retinopathy, NCT02388984, ClinicalTrials.gov.
Informed consent statement: All participants provided informed consent before enrollment.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
CONSORT 2010 statement: The authors have read the CONSORT 2010 statement, and the manuscript was prepared and revised according to the CONSORT 2010 statement.
Data sharing statement: No additional data are available.
Corresponding author: Xiao-Lin Tong, PhD, Metabolic Disease Research Institute, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, No. 5 North Line Pavilion, Xicheng District, Beijing 100053, China. tongxiaolin@vip.163.com
Received: September 9, 2025
Revised: October 20, 2025
Accepted: January 4, 2026
Published online: March 15, 2026
Processing time: 184 Days and 17.4 Hours
Abstract
BACKGROUND

Compound danshen dripping pill (CDDP), an approved treatment for non-proliferative diabetic retinopathy (NPDR) in China, has demonstrated potential in both preclinical and clinical studies. However, its efficacy in NPDR has not been validated through large clinical trials.

AIM

To evaluate the therapeutic efficacy and safety of CDDP in NPDR.

METHODS

This randomized, placebo-controlled, double-blind, multicenter study included 484 NPDR patients across 16 centers in China from November 2013 to July 2017. Eligible NPDR patients were randomly assigned to the CDDP and placebo groups at a ratio of 3:1. The intervention lasted for 24 weeks. The primary outcome was the overall effective rate of fundus changes at 24 weeks, assessed through retinal microvascular status, the number of hemorrhages, and exudation area. Secondary outcomes included retinopathy severity, traditional Chinese medicine (TCM) symptoms, macular edema, and corrected visual acuity. The full analysis set (FAS) included all enrolled cases who were randomized and administered at least one study drug.

RESULTS

Of the 484 randomized participants, 483 (362 and 121 in the CDDP and placebo groups, respectively) were included in the FAS. At 24 weeks, the overall effective rate in the CDDP group was 77.07%, significantly higher than 53.72% found in the placebo group (P < 0.001). Results remained consistent after adjusting for central effects and baseline HbA1c. Additionally, CDDP outperformed placebo in improving retinal lesion severity, microaneurysms, hemorrhages, diabetic macular edema, and TCM symptoms. The frequencies of adverse events detected by laboratory tests did not significantly differ between the two groups.

CONCLUSION

CDDP significantly and effectively alleviates NPDR. Future research should focus on assessing long-term outcomes.

Keywords: Diabetic retinopathy; Compound danshen dripping pills; Clinical trial; Efficacy; Safety

Core Tip: Compound danshen dripping pill (CDDP), an approved treatment for non-proliferative diabetic retinopathy (DR) in China, has demonstrated potential in both preclinical and clinical studies. However, its efficacy for non-proliferative DR (NPDR) has not been validated through large-scale clinical trials. We conducted this randomized, placebo-controlled, double-blind, multicenter study to confirm the therapeutic efficacy and safety of CDDP in NPDR.