Guangdong Provincial Hospital of Chinese Medicine, The Second Clinical School of Medicine, Guangzhou University of Chinese Medicine, Guangzhou and Zhuhai, China.
Guangdong Provincial Key Laboratory of Research on Emergency in Traditional Chinese Medicine, Emergency Department, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, China.
Trials. 2020 Mar 17;21(1):267. doi: 10.1186/s13063-020-4109-6.
Coronary heart disease (CHD) is a clinical syndrome caused by coronary atherosclerosis (AS) or functional changes in coronary arteries. We have previously reported that astragaloside IV (in astragalus) and tanshinone IIA (in Salvia miltiorrhiza) improve myocardial ischemic injury.
This study will employ the randomized, blinded, prospective, single-center experiments approach. Briefly, a total of 160 eligible patients will be equally randomized into three treatment groups and placebo control groups. Patients will receive appropriate treatments every 24 h for seven days after enrollment and followed up for 28 days. The main evaluation indicators will be cell count, serum high-sensitivity C-reactive protein (hs-CRP) level, monocyte chemoattractant protein 1 (MCP-1), interleukin-6 (IL-6), interleukin-1β (IL-1β), interleukin-8 (IL-8), interleukin-18 (IL-18), interleukin-10 (IL-10), tumor necrosis factor (TNF)-α, oxidized low density lipoprotein (OX-LDL), angina grade, and Traditional Chinese Medicine (TCM) symptom changes scale. Secondary indicators to be evaluated will include B-type natriuretic peptide (BNP) levels, troponin (cTn), muscle enzyme isoenzyme (CK-MB), heart-type fatty acid binding protein (H-FABP), liver and renal functions, as well as blood coagulation. Close monitoring of adverse events during the trial will also be conducted.
This randomized controlled trial of Chinese herbal extracts for the treatment of coronary heart disease will generate results that are expected to provide valuable clinical evidence to inform future development of therapies towards management of CHD.
China Clinical Trial Registration Center, ChiCTR1900021590. Registered on 28 February 2019.
冠心病(CHD)是由冠状动脉粥样硬化(AS)或冠状动脉功能变化引起的临床综合征。我们之前报道过黄芪甲苷(黄芪)和丹参酮 IIA(丹参)可改善心肌缺血损伤。
本研究将采用随机、盲法、前瞻性、单中心试验方法。简而言之,将总共 160 名符合条件的患者等分为三组治疗组和安慰剂对照组。患者将在入组后每 24 小时接受一次适当的治疗,持续 7 天,并随访 28 天。主要评价指标将是细胞计数、血清高敏 C 反应蛋白(hs-CRP)水平、单核细胞趋化蛋白 1(MCP-1)、白细胞介素 6(IL-6)、白细胞介素 1β(IL-1β)、白细胞介素 8(IL-8)、白细胞介素 18(IL-18)、白细胞介素 10(IL-10)、肿瘤坏死因子(TNF)-α、氧化型低密度脂蛋白(OX-LDL)、心绞痛分级和中医(TCM)症状变化量表。次要评价指标将包括 B 型利钠肽(BNP)水平、肌钙蛋白(cTn)、肌酶同工酶(CK-MB)、心肌型脂肪酸结合蛋白(H-FABP)、肝肾功能以及凝血功能。试验期间还将密切监测不良事件。
这项中药提取物治疗冠心病的随机对照试验将产生预期的结果,为未来治疗冠心病的发展提供有价值的临床证据。
中国临床试验注册中心,ChiCTR1900021590。于 2019 年 2 月 28 日注册。