Department of Cardiology, Key Laboratory of Cardiovascular Intervention and Regenerative Medicine of Zhejiang Province, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, 3 East Qingchun Road, Hangzhou, Zhejiang, 310016, P.R. China.
BMC Cardiovasc Disord. 2020 Jun 5;20(1):273. doi: 10.1186/s12872-020-01557-3.
Trimetazidine is a metabolic anti-ischemic agent, which increases the tolerance of cardiomyocytes to ischemia. However, few studies have explored the effect of trimetazidine on ventricular remodeling in coronary artery disease (CAD) patients undergoing percutaneous coronary intervention (PCI) with left ventricular hypertrophy (LVH).
It is a randomized, placebo-controlled trial, and we propose to recruit one hundred and twenty-four CAD patients undergoing PCI with LVH during a 12-month period. They will be randomized to receive either trimetazidine (35 mg twice a day) or placebo in the following 12 months after PCI. Blood tests, echocardiography, symptom of angina and major adverse cardiovascular events (MACEs) will be collected at follow-up visit at 3 and 12 months. The primary end point will be the left ventricular remodeling measured by left ventricular mass index (LVMI) at 3- and 12-month follow-up compared with the baseline. The secondary end points will be the symptom of angina assessed by Seattle Angina Questionnaire, myocardial ischemia measured by 6-min walk test and exercise electrocardiography test, as well as MACEs (defined as a composite of death, myocardial infarction, stroke, recurrent angina, re-hospitalization, change of viable myocardium).
This study aims to demonstrate the effect of trimetazidine on left ventricular remodeling and myocardial ischemia in CAD patients undergoing PCI with LVH. Trimetazidine treatment is likely to improve the left ventricular remodeling, symptoms of angina and myocardial ischemia. It might also reduce the risk of MACEs in CAD patients undergoing PCI with LVH.
http://www.chictr.org.cn, Chinese Clinical Trial Registry (ChiCTR1800017876). Registered on 19 Aug 2018.
曲美他嗪是一种代谢性抗缺血药物,可提高心肌细胞对缺血的耐受性。然而,很少有研究探讨曲美他嗪对经皮冠状动脉介入治疗(PCI)合并左心室肥厚(LVH)的冠心病(CAD)患者心室重构的影响。
这是一项随机、安慰剂对照试验,我们计划在 12 个月内招募 124 名经 PCI 合并 LVH 的 CAD 患者。他们将在 PCI 后 12 个月内随机接受曲美他嗪(每天两次,每次 35mg)或安慰剂治疗。在 3 个月和 12 个月的随访时,将采集血样、超声心动图、心绞痛症状和主要不良心血管事件(MACEs)。主要终点是与基线相比,在 3 个月和 12 个月随访时通过左心室质量指数(LVMI)测量的左心室重构。次要终点是西雅图心绞痛问卷评估的心绞痛症状、6 分钟步行试验和运动心电图测量的心肌缺血以及 MACEs(定义为死亡、心肌梗死、中风、复发性心绞痛、再住院、存活心肌变化的复合事件)。
本研究旨在证明曲美他嗪对经 PCI 合并 LVH 的 CAD 患者左心室重构和心肌缺血的影响。曲美他嗪治疗可能改善左心室重构、心绞痛症状和心肌缺血。它还可能降低经 PCI 合并 LVH 的 CAD 患者的 MACEs 风险。
http://www.chictr.org.cn,中国临床试验注册中心(ChiCTR1800017876)。于 2018 年 8 月 19 日注册。