针灸作为 STEMI 患者 PCI 后辅助治疗的效果和安全性:随机对照试验研究方案。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yi Zhao, Fayang Ling, Yalu Qin, Wen Xie, Wenchuan Qi, Qian Nie, Hongcai Zhang, Mingjun Han, Jue Zhao, Lei Liu, Lin Hu, Juan Xiao, Wufeng Li, Fanrong Liang, Qianhua Zheng
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引用次数: 0

摘要

背景:ST段抬高型心肌梗死(STEMI)是一种常见的急性缺血性心脏病,对全球人类健康造成严重损害。尽管经皮冠状动脉介入治疗(PCI)已大大降低了发病率和死亡率,但仍需要额外的心脏保护策略。在最近的许多研究中,针灸疗法对心脏保护起着主导作用。因此,我们旨在通过一项随机对照试验,评估针灸作为一种辅助疗法对 STEMI 患者进行 PCI 治疗的效果和安全性:本研究描述了一项多中心、双盲、平行对照、随机对照试验方案。研究将从成都中医药大学附属医院、成都中医药大学附属第三医院/成都市郫都区中医院和昭通市中医院招募 96 名接受 PCI 治疗的 STEMI 患者,年龄在 18-85 岁之间。参与者将按 1:1 的比例被随机分配到真针刺加基础疗法组(即治疗组)或假针刺加基础疗法组(即对照组)。这些参与者将接受为期 5 天的治疗,然后接受 24 周的随访。在整个研究过程中将记录任何不良反应,以评估安全性:本研究旨在探讨针灸治疗PCI术后STEMI患者的效果和安全性,并为这些患者建立标准化的针灸治疗方案:本研究于2024年2月22日在中国临床试验注册中心注册(注册号:[ChiCTR2400081117])。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect and safety of acupuncture as adjunctive therapy for STEMI patients after PCI: study protocol of a randomized controlled trial.

Background: ST-elevation myocardial infarction (STEMI) is a common acute ischemia heart disease that causes serious damage to human health worldwide. Even though morbidity and mortality have significantly decreased by percutaneous coronary intervention (PCI), an additional cardiac protection strategy is still required. Acupuncture therapy has presented a dominant cardiac protection in many studies lately. Thus, we aim to evaluate the effect and safety of acupuncture as an adjunctive therapy in STEMI patients after PCI through a randomized controlled trial.

Methods/design: This study describes a protocol of multicenter, double-blinded, parallel-controlled, randomized controlled trial. Ninety-six patients with STEMI aged 18-85 years who undergoing PCI will be recruited from the Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, The Affiliated Third Hospital of Chengdu Traditional Chinese Medicine University/Chengdu Pidu District Hospital of Traditional Chinese Medicine, and Zhaotong Municipal Hospital of Traditional Chinese Medicine. Participants will be randomly assigned (1:1 ratio) to the verum acupuncture plus basic therapy (i.e., treatment) group or the sham acupuncture plus basic therapy (i.e., control) group. These participants will be treated for 5 days and then will be followed up for 24 weeks. Any adverse events will be recorded throughout the study to evaluate safety.

Discussion: The present study aims to investigate the effect and safety of acupuncture for patients with STEMI after PCI and set up standardized treatment programs for acupuncture of these patients.

Trial registration: This study was registered in the Chinese Clinical Trial Registry (Registration ID: [ChiCTR2400081117]), on February 22, 2024.

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CiteScore
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