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中药参芪化瘀方治疗糖尿病下肢动脉疾病患者的疗效和安全性:一项多中心、随机、双盲、安慰剂对照试验的研究方案

The efficacy and safety of Chinese herbal medicine Shen-Qi Hua-Yu formula in patients with diabetic lower extremity artery disease: Study protocol of a multi-center, randomized, double-blind, placebo-controlled trial.

作者信息

Leng Yulin, Gao Hong, Fu Xiaoxu, Xie Hongyan, Hu Zhipeng, Zhu Jianwei, Liu Xiaoke, Zhou Xiujuan, Xie Ziyan, Xie Chunguang

机构信息

Hospital of Chengdu University of Traditional Chinese Medicine, PR China.

出版信息

Medicine (Baltimore). 2020 Jan;99(3):e18713. doi: 10.1097/MD.0000000000018713.

Abstract

BACKGROUND

Lower extremity artery disease (LEAD) is greatly harmful to Type 2 Diabetes Mellitus patients. Traditional Chinese Medicine (TCM) is an alternative therapy to delay the development of macrovascular diseases, but the existing evidence of its efficacy, safety and mechanism of action is insufficient. We report a study protocol of a multi-center, randomized, double-blind, placebo-controlled trial that aims to use well-designed clinical trial to evaluate the efficacy and safety of Chinese herbal medicine (CHM) Shen-Qi Hua-Yu formula, and to explore efficacy mechanism of the TCM granules and the biomarkers of TCM syndrome.

METHODS

This is a multi-center, double-blind, randomized, and placebo-controlled study that randomized 120 participants into 2 groups. The treatment group will receive TCM granules and conventional medicine, while the control group will receive placebo in addition to conventional medicine. Two groups will receive 12-week treatment and 48-week follow-up, with a total of 13 visits. Primary efficacy outcomes included ankle brachial index. Secondary efficacy outcomes included fasting plasma glucose, blood lipid, hemorheology indexes, advanced glycation end products, the inner diameter, peak systolic velocity, end diastolic velocity and mean average velocity of the anterior tibial artery, posterior tibial artery and dorsalis pedis artery, and TCM syndrome score. The safety and endpoint outcomes will be evaluated in this trial. The study will explain the biological therapeutic mechanism of Shen-Qi Hua-Yu formula for diabetic LEAD, and try to use Isobaric tags for Relative and Absolute Quantitation (iTRAQ) and Western blot to screen biomarkers of characteristic diagnosis and clinical efficiency evaluation of the TCM syndrome.

DISCUSSION

This study is a multi-center, randomized, double-blind, placebo-controlled trial to evaluate the efficacy and safety of CHM in patients with diabetic LEAD, and to interpret the therapeutic mechanism of Shen-Qi Hua-Yu formula in treatment of diabetic LEAD through proteomics technology, and to screen biomarkers with characteristics of TCM diagnosis and clinical efficacy evaluation. On the other hand, to our knowledge, this study may be the first trial of CHM formulas to observe cardiovascular outcomes through long-term follow-up for the treatment of diabetic LEAD, which is of great value.

TRIAL REGISTRATION

This study is registered on the Chinese Clinical Trial Registry: ChiCTR1900026372.

摘要

背景

下肢动脉疾病(LEAD)对2型糖尿病患者危害极大。中医药是延缓大血管疾病发展的一种替代疗法,但现有关于其疗效、安全性及作用机制的证据不足。我们报告一项多中心、随机、双盲、安慰剂对照试验的研究方案,旨在通过精心设计的临床试验评估中药(CHM)参芪化瘀方的疗效和安全性,并探索中药颗粒剂的疗效机制及中医证候生物标志物。

方法

这是一项多中心、双盲、随机、安慰剂对照研究,将120名参与者随机分为2组。治疗组将接受中药颗粒剂和常规药物,而对照组除常规药物外将接受安慰剂。两组将接受12周治疗和48周随访,共13次就诊。主要疗效指标包括踝臂指数。次要疗效指标包括空腹血糖、血脂、血液流变学指标、晚期糖基化终产物、胫前动脉、胫后动脉和足背动脉的内径、收缩期峰值流速、舒张末期流速和平均流速,以及中医证候评分。本试验将评估安全性和终点指标。该研究将阐释参芪化瘀方治疗糖尿病性LEAD的生物学治疗机制,并尝试使用相对与绝对定量同位素标记(iTRAQ)和蛋白质印迹法筛选中医证候特征性诊断和临床疗效评估的生物标志物。

讨论

本研究是一项多中心、随机、双盲、安慰剂对照试验,旨在评估中药治疗糖尿病性LEAD患者的疗效和安全性,并通过蛋白质组学技术阐释参芪化瘀方治疗糖尿病性LEAD的治疗机制,筛选具有中医诊断和临床疗效评估特征的生物标志物。另一方面,据我们所知,本研究可能是首个通过长期随访观察心血管结局以治疗糖尿病性LEAD的中药方剂试验,具有重要价值。

试验注册

本研究已在中国临床试验注册中心注册:ChiCTR1900026372。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee3/7220098/b4b44058590a/medi-99-e18713-g001.jpg

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