如意珍宝片和白芨膏治疗急性缺血性脑卒中:多中心、随机、双盲、平行对照试验研究方案》。

Biomedicine hub Pub Date : 2024-06-10 eCollection Date: 2024-01-01 DOI:10.1159/000538704
Xinzuo Qin, Liyuan Huang, Haiyue Zhang, Zijian Wang, Xiao Wu, Cuomu Mingji, Qi Wan, Haiqing Song, Juexian Song
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引用次数: 0

摘要

简介脑卒中具有发病率高、复发率高和死亡率高的特点。不符合急性血管重建治疗条件的急性缺血性脑卒中(AIS)患者需要更有效的药物治疗。此前的一项临床研究显示,如意珍宝片和白马贴膏可能对 AIS 有效,但目前尚缺乏高质量的临床证据支持其在 AIS 中的应用。为了探索这两种经典藏药治疗 AIS 的疗效,我们将对不符合溶栓治疗条件的 AIS 患者进行随机临床试验:方法:将进行一项前瞻性、随机、多中心、双盲、安慰剂对照和平行组试验。我们将把 480 名符合条件的参与者随机分配到干预组或对照组。各组的分配比例为 1:1:1:1:1,其中包括双药组、白豆蔻软膏组、如意珍宝片组和安慰剂组各 120 名患者。参与者将接受为期 8 周的药物治疗,并在开始治疗后的 4 周(D29)、8 周(D56)和 90 天(D90)接受三次随访。主要结果是简化 Fugl-Meyer 评分从基线到治疗后 90 天的变化。次要结果如下D29简化版Fugl-Meyer评分从基线到治疗后的变化;D29 NIHSS评分比基线下降4分或更多的受试者比例;D90 mRS评分为0-2分(含)的受试者比例;D90 Barthel指数评分≥95分的受试者比例;D90心脑血管事件发生率。安全性终点包括 90 天内的死亡率;90 天内发生不良事件/严重不良事件的受试者比例:该研究方案为实际执行奠定了坚实的基础。这项研究将为其他藏医药研究人员提供参考,为降低全球中风相关支出做出贡献,进而造福更多的中风患者。
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Ruyi Zhenbao Tablet and Baimai Ointment Therapy in Acute Ischemic Stroke: A Study Protocol for a Multi-Center, Randomized, Double-blinded, and Parallel-Controlled Trial.

Introduction: Stroke is characterized by high incidence, recurrence rate, and mortality. Patients with acute ischemic stroke (AIS) who are ineligible for acute revascularization therapy require more effective medication treatments. A previous clinical study showed that Ruyi Zhenbao tablets and Baimai ointments might be effective against AIS; however, high-quality clinical evidence supporting their application in AIS is lacking. To explore the efficacy of the two classic Tibetan medicines in the treatment of AIS, a randomized clinical trial will be conducted in patients with AIS who are not eligible for thrombolytic treatment.

Methods: A prospective, randomized, multiple-center, double-blinded, placebo-controlled, and parallel-group trial will be conducted. We shall randomize 480 eligible participants to either the intervention or the control group. The distribution ratio of each group will be 1:1:1:1, including 120 patients each in the dual-medication group, the Baimai ointment group, the Ruyi Zhenbao tablet group, and the placebo group. Participants will be treated with medication for 8 weeks, and they will receive three follow-up visits: at 4 weeks (D29), 8 weeks (D56), and 90 days (D90) after commencing treatment. The primary outcome will be D90 change in the simplified Fugl-Meyer score from baseline to posttreatment. The secondary outcomes are as follows: D29 change of simplified Fugl-Meyer score from baseline to posttreatment; proportion of participants whose D29 NIHSS scores decreased by four or more points from baseline D90 proportion of subjects with mRS score of 0-2 (inclusive); D90 proportion of subjects with Barthel index score ≥95; D90 incidence of cardiovascular and cerebrovascular events. Safety endpoint includes mortality within 90 days; proportion of subjects with adverse events/serious adverse events within 90 days.

Conclusion: This research protocol lays a solid groundwork for its practical execution. This study is poised to serve as a reference for other Tibetan medicine researchers, contributing to the reduction of stroke-related expenditures globally and, in turn, benefiting a broader population of stroke patients.

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