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Chinese medicine neuroaid efficacy on stroke recovery: a double-blind, placebo-controlled, randomized study

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dc.contributor.author Chen, C.L. en_US
dc.contributor.author Young, S.H. en_US
dc.contributor.author Gan, H.H. en_US
dc.contributor.author Singh, R. en_US
dc.contributor.author Lao, A.Y. en_US
dc.contributor.author Baroque, A.C. en_US
dc.contributor.author Chang, H.M. en_US
dc.contributor.author Hiyadan, J.H. en_US
dc.contributor.author Chua, C.L. en_US
dc.contributor.author Advincula, J.M. en_US
dc.contributor.author Muengtaweepongsa, S. en_US
dc.contributor.author Chan, B.P. en_US
dc.contributor.author de Silva, H.A. en_US
dc.contributor.author Towanabut, S. en_US
dc.contributor.author Suwanwela, N.C. en_US
dc.contributor.author Poungvarin, N. en_US
dc.contributor.author Chankrachang, S. en_US
dc.contributor.author Wong, K.S. en_US
dc.contributor.author Eow, G.B. en_US
dc.contributor.author Navarro, J.C. en_US
dc.contributor.author Venketasubramanian, N. en_US
dc.contributor.author Lee, C.F. en_US
dc.contributor.author Bousser, M.G. en_US
dc.contributor.author CHIMES Study Investigators en_US
dc.date.accessioned 2014-10-29T09:40:20Z en_US
dc.date.available 2014-10-29T09:40:20Z en_US
dc.date.issued 2013 en_US
dc.identifier.citation Stroke. 2013; 44(8): 2093-100 [Epub 2013 Jun 18.] en_US
dc.identifier.issn 0039-2499 (Print) en_US
dc.identifier.issn 1524-4628 (Electronic) en_US
dc.identifier.other 10.1161/STROKEAHA.113.002055. en
dc.identifier.other http://stroke.ahajournals.org/content/44/8/2093.long en
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/2222 en
dc.description.abstract BACKGROUND AND PURPOSE: Previous clinical studies suggested benefit for post stroke 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. en_US
dc.publisher Lippincott Williams and Wilkins en_US
dc.title Chinese medicine neuroaid efficacy on stroke recovery: a double-blind, placebo-controlled, randomized study en_US
dc.type Article en_US
dc.identifier.department Pharmacology en_US
dc.creator.corporateauthor American Heart Association en_US
dc.description.note Indexed in MEDLINE en_US


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