首页> 外文期刊>Trials >Efficacy and safety of Suxiao Jiuxin Pill in the treatment of stable angina (Qi stagnation and blood stasis syndrome): study protocol of a randomized, double-blind, placebo-controlled, multi-center clinical trial
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Efficacy and safety of Suxiao Jiuxin Pill in the treatment of stable angina (Qi stagnation and blood stasis syndrome): study protocol of a randomized, double-blind, placebo-controlled, multi-center clinical trial

机译:Suxiao Jiuxin丸治疗稳定心绞痛(气停滞与血瘀综合征)的疗效和安全性:随机,双盲,安慰剂控制,多中心临床试验研究方案

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Coronary heart disease (CHD) has become one of the biggest health problems in the world. Stable angina is a common clinical type of CHD with poor prognosis and high mortality. Although there are various interventions for stable angina, none of them can significantly reduce mortality. Both basic and clinical research have shown that Suxiao Jiuxin Pill (SJP) can relieve the symptoms of angina pectoris and improve the clinical efficacy, but there is a lack of high-quality clinical research to provide research-based evidence. We design a randomized, double-blind, placebo-controlled trial to evaluate the efficacy of SJP for stable angina. This is a prospective, randomized, double-blind, placebo-controlled, and multicenter trial. The trial will enroll 324 participants with chronic stable angina (Qi Stagnation and Blood Stasis syndrome). All participants will have received the conventional therapy of chronic stable angina. Participants will be randomized into two groups, conventional therapy plus SJP group and conventional therapy plus placebo group. Eligible participants will receive either SJP or placebo (five pills administered orally, three times daily) in addition to conventional treatment for 24?weeks. The primary outcomes are the symptom improvement rate of angina from baseline to 4?weeks after inclusion and major adverse cardiovascular events (MACE). The secondary outcomes are angina classification (CCS), improvement of traditional Chinese medicine (TCM) syndromes, Seattle Angina Scale score, the dosage of emergency drugs and the stopping rate, and electrocardiogram (EKG) efficacy. Adverse events will be monitored throughout the trial. Integrated traditional Chinese and Western Medicine is commonly used for angina in China. This study will evaluate the clinical effectiveness and safety of SJP for angina. The results of the trial will provide high-level clinical research-based evidence for the application of SJP instable angina. This study protocol was registered on 14 March 2019. The registration number is ChiCTR1900021876 on the Chinese Clinical Trial Registry.
机译:冠心病(CHD)已成为世界上最大的健康问题之一。稳定的心绞痛是一种常见的临床类型的CHD,预后差和高死亡率。虽然稳定的心绞痛有各种干预措施,但它们都没有明显减少死亡率。基本和临床研究都表明,遂夏朱祥丸(SJP)可以缓解心绞痛症的症状,提高临床疗效,但缺乏高质量的临床研究,以提供基于研究的证据。我们设计随机,双盲,安慰剂对照试验,以评估SJP对稳定心绞痛的功效。这是一个预期,随机,双盲,安慰剂控制和多中心试验。该试验将注册324名与慢性稳定心绞痛(QI停滞和血瘀综合征)的参与者。所有参与者都将接受常规治疗慢性稳定心绞痛。参与者将随机分为两组,常规治疗加SJP组和常规治疗加安慰剂组。除常规治疗24个星期外,符合条件的参与者将收到SJP或安慰剂(每日口服给药,每日三次)。主要结果是血缘的症状改善率从基线到4?包裹后的3周,主要的不良心血管事件(MACE)。二次结果是心绞痛分类(CCS),改善中医(TCM)综合征,西雅图angina比分评分,应急药物剂量和停止率,以及心电图(EKG)疗效。在整个审判中将监测不良事件。综合中西部和西医普遍用于中国心绞痛。本研究将评估SJP对心绞痛的临床效果和安全性。试验结果将为SJP稳定心绞痛提供高级别的临床研究基础证据。本研究议定书于2019年3月14日登记。注册号是中国临床试验登记处的CHICTR1900021876。

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