Chinese Medicine Neuroaid Efficacy on Stroke Recovery A Double-Blind, Placebo-Controlled, Randomized Study

被引:94
作者
Chen, Christopher L. H. [1 ]
Young, Sherry H. Y. [2 ]
Gan, Herminigildo H. [3 ]
Singh, Rajinder [4 ]
Lao, Annabelle Y. [5 ]
Baroque, Alejandro C. [6 ]
Chang, Hui Meng [7 ]
Hiyadan, John Harold B. [8 ]
Chua, Carlos L. [9 ]
Advincula, Joel M. [10 ]
Muengtaweepongsa, Sombat [11 ]
Chan, Bernard P. L. [12 ]
de Silva, H. Asita [13 ]
Towanabut, Somchai [14 ]
Suwanwela, Nijasri C. [15 ]
Poungvarin, Niphon [16 ]
Chankrachang, Siwaporn [17 ]
Wong, K. S. Lawrence [18 ]
Eow, Gaik Bee [19 ]
Navarro, Jose C. [20 ]
Venketasubramanian, Narayanaswamy [21 ]
Lee, Chun Fan [22 ]
Bousser, Marie-Germaine [23 ]
机构
[1] Natl Univ Singapore, Dept Pharmacol, Clin Res Ctr, Singapore 117597, Singapore
[2] Changi Gen Hosp, Singapore, Singapore
[3] Jose Reyes Mem Med Ctr, Manila, Philippines
[4] Natl Inst Neurosci, Singapore, Singapore
[5] San Pedro Hosp, Davao Med Sch Fdn Hosp, Davao, Philippines
[6] Univ Santo Tomas Hosp, Manila, Philippines
[7] Singapore Gen Hosp, Natl Neurosci Inst, Singapore, Singapore
[8] Baguio Gen Hosp & Med Ctr, Baguio, Philippines
[9] Univ Philippines Manila, Philippine Gen Hosp, Manila, Philippines
[10] West Visayas State Univ Med Ctr, Lapaz, Philippines
[11] Thammasat Univ, Pathum Thani, Thailand
[12] Natl Univ Hlth Syst, Natl Univ Hosp, Div Neurol, Singapore, Singapore
[13] Univ Kelaniya, Fac Med, Dept Pharmacol, Clin Trials Unit, Ragama, Sri Lanka
[14] Prasat Neurol Inst, Rajthevi Bangkok, Thailand
[15] Chulalongkorn Univ, Fac Med, Div Neurol, Bangkok 10330, Thailand
[16] Siriraj Hosp, Bangkok, Thailand
[17] Chiang Mai Univ, Chiang Mai 50000, Thailand
[18] Chinese Univ Hong Kong, Prince Wales Hosp, Shatin, Hong Kong, Peoples R China
[19] Penang Hosp, Georgetown, Penang, Malaysia
[20] Univ Santo Tomas Hosp, Manila, Philippines
[21] Raffles Hosp, Raffles Neurosci Ctr, Singapore, Singapore
[22] Singapore Clin Res Inst, Singapore, Singapore
[23] Lariboisiere Univ Hosp, Paris, France
基金
英国医学研究理事会;
关键词
clinical trial; medicine; Chinese traditional; NeuroAiD; stroke; acute; recovery of function; ACUTE ISCHEMIC-STROKE; MLC601 NEUROAID(R); MULTICENTER; INVESTIGATE; MLC901; INFARCT; SAFETY; BRAIN;
D O I
10.1161/STROKEAHA.113.002055
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background and Purpose Previous clinical studies suggested benefit for poststroke recovery when MLC601 was administered between 2 weeks and 6 months of stroke onset. The Chinese Medicine Neuroaid Efficacy on Stroke recovery (CHIMES) study tested the hypothesis that MLC601 is superior to placebo in acute, moderately severe ischemic stroke within a 72-hour time window. Methods This multicenter, double-blind, placebo-controlled trial randomized 1100 patients with a National Institutes of Health Stroke Scale score 6 to 14, within 72 hours of onset, to trial medications for 3 months. The primary outcome was a shift in the modified Rankin Scale. Secondary outcomes were modified Rankin Scale dichotomy, National Institutes of Health Stroke Scale improvement, difference in National Institutes of Health Stroke Scale total and motor scores, Barthel index, and mini-mental state examination. Planned subgroup analyses were performed according to age, sex, time to first dose, baseline National Institutes of Health Stroke Scale, presence of cortical signs, and antiplatelet use. Results The modified Rankin Scale shift analysis-adjusted odds ratio was 1.09 (95% confidence interval, 0.86-1.32). Statistical difference was not detected between the treatment groups for any of the secondary outcomes. Subgroup analyses showed no statistical heterogeneity for the primary outcome; however, a trend toward benefit in the subgroup receiving treatment beyond 48 hours from stroke onset was noted. Serious and nonserious adverse events rates were similar between the 2 groups. Conclusions MLC601 is statistically no better than placebo in improving outcomes at 3 months when used among patients with acute ischemic stroke of intermediate severity. Longer treatment duration and follow-up of participants with treatment initiated after 48 hours may be considered in future studies. Clinical Trial Registration URL: http://www.clinicaltrials.gov. Unique identifier: NCT00554723.
引用
收藏
页码:2093 / 2100
页数:8
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