TXL-CAP试验的研究设计和基本原理:一项随机、双盲、安慰剂对照、多中心临床试验,评估通心络胶囊对冠状动脉粥样硬化斑块稳定性的影响。

IF 2.6 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Mei Ni, Yun Ti, Yan Qi, Meng Zhang, Dayue Darrel Duan, Chen Yao, Zhen-Hua Jia, Yun Zhang, Pei-Li Bu
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引用次数: 0

摘要

最近的临床试验表明,中药通心络胶囊对动脉粥样硬化有保护作用。然而,TXL治疗对冠状动脉斑块易损影响的临床证据尚不清楚。因此,我们开展了这项研究,探讨在他汀类药物治疗的基础上,TXL胶囊治疗可能稳定急性冠脉综合征(ACS)患者的冠状动脉病变的假设。TXL-CAP研究是一项研究者发起的、随机的、双盲的临床试验,在中国18个医疗中心进行。研究招募年龄在18 ~ 80岁的ACS患者,这些患者的非介入性冠状动脉靶病变纤维帽厚度(FCT) < 100 μm,脂质弧> 90°,由光学相干断层扫描(OCT)定义。最终将招募220名符合选择标准但不符合排除标准的患者,并随机接受TXL (n = 110)或安慰剂(n = 110)治疗,为期12个月。主要终点是在12个月的随访结束时,TXL组和安慰剂组冠状动脉靶病变最小FCT的差异。次要终点包括:(1)12个月结束时目标斑块最大脂质弧和长度的变化,以及脂质斑块、纤维斑块和钙化斑块的百分比;(2) 12个月内复合心血管事件和冠状动脉血运重建术的发生率;(3)分别采用加拿大心血管学会(CCS)分级系统和西雅图心绞痛问卷(SAQ)评分评估心绞痛等级和评分的变化;(4)血清hs-CRP水平变化。TXL- cap试验的结果将为揭示TXL胶囊是否能稳定中国ACS患者的冠状动脉易损斑块提供额外的临床数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study design and rationale of the TXL-CAP trial: a randomized, double-blind, placebo-controlled, multicenter clinical trial assessing the effect of Tongxinluo capsules on the stability of coronary atherosclerotic plaques.

Recent clinical trials have demonstrated a protective effect in using traditional Chinese medicine Tongxinluo (TXL) capsule to treat atherosclerosis. However, clinical evidence of the effects of TXL treatment on coronary plaque vulnerability is unavailable. In response, we developed this study to investigate the hypothesis that on the basis of statin therapy, treatment with TXL capsule may stabilize coronary lesions in patients with acute coronary syndrome (ACS). The TXL-CAP study was an investigator-initiated, randomized, double-blind clinical trial conducted across 18 medical centers in China. Patients with ACS aging from 18 to 80 years old who had a non-intervened coronary target lesion with a fibrous cap thickness (FCT) < 100 μm and lipid arc > 90° as defined by optical coherence tomography (OCT) were recruited. A total of 220 patients who met the selection criteria but did not meet the exclusion criteria will be finally recruited and randomized to receive treatment with TXL (n = 110) or placebo (n = 110) for a duration of 12 months. The primary endpoint was the difference in the minimum FCT of the coronary target lesion between TXL and placebo groups at the end of the 12-month follow-up. Secondary endpoints included: (1) changes of the maximum lipid arc and length of the target plaque, and the percentage of lipid, fibrous, and calcified plaques at the end of the 12-month period; (2) the incidence of composite cardiovascular events and coronary revascularization within the 12 months; (3) changes in the grade and scores of the angina pectoris as assessed using the Canadian Cardiovascular Society (CCS) grading system and Seattle angina questionnaire (SAQ) score, respectively; and (4) changes in hs-CRP serum levels. The results of the TXL-CAP trial will provide additional clinical data for revealing whether TXL capsules stabilizes coronary vulnerable plaques in Chinese ACS patients.

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来源期刊
Journal of Geriatric Cardiology
Journal of Geriatric Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-GERIATRICS & GERONTOLOGY
CiteScore
3.30
自引率
4.00%
发文量
1161
期刊介绍: JGC focuses on both basic research and clinical practice to the diagnosis and treatment of cardiovascular disease in the aged people, especially those with concomitant disease of other major organ-systems, such as the lungs, the kidneys, liver, central nervous system, gastrointestinal tract or endocrinology, etc.
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