Qin Xinzuo, Huang Liyuan, Zhang Haiyue, Wang Zijian, Wu Xiao, Mingji Cuomu, Wan Qi, Song Haiqing, Song Juexian
Department of Neurology, Xuanwu Hospital, Capital Medical University, National Center for Neurological Disorders, Beijing, China.
Postgraduate Department, The University of Tibetan Medicine in Lhasa, Lhasa, China.
Biomed Hub. 2024 Jun 10;9(1):94-107. doi: 10.1159/000538704. eCollection 2024 Jan-Dec.
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.
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.
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.
中风具有高发病率、复发率和死亡率的特点。不符合急性血管再通治疗条件的急性缺血性中风(AIS)患者需要更有效的药物治疗。先前的一项临床研究表明,如意珍宝片和白脉软膏可能对AIS有效;然而,缺乏支持它们在AIS中应用的高质量临床证据。为了探索这两种经典藏药治疗AIS的疗效,将对不符合溶栓治疗条件的AIS患者进行一项随机临床试验。
将进行一项前瞻性、随机、多中心、双盲、安慰剂对照的平行组试验。我们将把480名符合条件的参与者随机分为干预组或对照组。每组的分配比例为1:1:1:1,双药组、白脉软膏组、如意珍宝片组和安慰剂组各120名患者。参与者将接受8周的药物治疗,并在开始治疗后的4周(第29天)、8周(第56天)和90天(第90天)接受三次随访。主要结局将是从基线到治疗后第90天简化Fugl-Meyer评分的变化。次要结局如下:从基线到治疗后第29天简化Fugl-Meyer评分的变化;第29天美国国立卫生研究院卒中量表(NIHSS)评分较基线下降4分或更多分的参与者比例;第90天改良Rankin量表(mRS)评分为0至2(含)的受试者比例;第90天巴氏指数评分≥95的受试者比例;第90天心血管和脑血管事件的发生率。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。
本研究方案为其实际实施奠定了坚实基础。本研究有望为其他藏药研究人员提供参考,有助于在全球范围内减少与中风相关的支出,进而使更多中风患者受益。