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Chinese medicine NeuroAiD efficacy on stroke recovery - extension study (CHIMES-E): A multicenter study of long-term efficacy

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dc.contributor.author Venketasubramanian, N.
dc.contributor.author Young, S.H.
dc.contributor.author Tay, S.S.
dc.contributor.author Umapathi, T.
dc.contributor.author Lao, A.Y.
dc.contributor.author Gan, H.H.
dc.contributor.author Baroque II, A.C.
dc.contributor.author Navarro, J.C.
dc.contributor.author Chang, H.M.
dc.contributor.author Advincula, J.M.
dc.contributor.author Muengtaweepongsa, S.
dc.contributor.author Chan, B.P.
dc.contributor.author Chua, C.L.
dc.contributor.author Wijekoon, N.
dc.contributor.author de Silva, H.A.
dc.contributor.author Hiyadan, J.H.
dc.contributor.author Suwanwela, N.C.
dc.contributor.author Wong, K.S.
dc.contributor.author Poungvarin, N.
dc.contributor.author Eow, G.B.
dc.contributor.author Lee, C.F.
dc.contributor.author Chen, C.L.
dc.date.accessioned 2015-08-06T06:53:43Z
dc.date.available 2015-08-06T06:53:43Z
dc.date.issued 2015
dc.identifier.citation Cerebrovascular Diseases.2015;39(5-6)1:309-18 en_US
dc.identifier.issn 1015-9770 (Print)
dc.identifier.issn 1421-9786 (Online)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/9150
dc.description.abstract BACKGROUND: The CHInese Medicine NeuroAiD Efficacy on Stroke recovery (CHIMES) study was an international randomized double-blind placebo-controlled trial of MLC601 (NeuroAiD) in subjects with cerebral infarction of intermediate severity within 72 h. CHIMES-E (Extension) aimed at evaluating the effects of the initial 3-month treatment with MLC601 on long-term outcome for up to 2 years. METHODS: All subjects randomized in CHIMES were eligible for CHIMES-E. Inclusion criteria for CHIMES were age ≥18, baseline National Institute of Health Stroke Scale of 6-14, and pre-stroke modified Rankin Scale (mRS) ≤1. Initial CHIMES treatment allocation blinding was maintained, although no further study treatment was provided in CHIMES-E. Subjects received standard care and rehabilitation as prescribed by the treating physician. mRS, Barthel Index (BI), and occurrence of medical events were ascertained at months 6, 12, 18, and 24. The primary outcome was mRS at 24 months. Secondary outcomes were mRS and BI at other time points. RESULTS: CHIMES-E included 880 subjects (mean age 61.8 ± 11.3; 36% women). Adjusted OR for mRS ordinal analysis was 1.08 (95% CI 0.85-1.37, p = 0.543) and mRS dichotomy ≤1 was 1.29 (95% CI 0.96-1.74, p = 0.093) at 24 months. However, the treatment effect was significantly in favor of MLC601 for mRS dichotomy ≤1 at 6 months (OR 1.49, 95% CI 1.11-2.01, p = 0.008), 12 months (OR 1.41, 95% CI 1.05-1.90, p = 0.023), and 18 months (OR 1.36, 95% CI 1.01-1.83, p = 0.045), and for BI dichotomy ≥95 at 6 months (OR 1.55, 95% CI 1.14-2.10, p = 0.005) but not at other time points. Subgroup analyses showed no treatment heterogeneity. Rates of death and occurrence of vascular and other medical events were similar between groups. CONCLUSIONS: While the benefits of a 3-month treatment with MLC601 did not reach statistical significance for the primary endpoint at 2 years, the odds of functional independence defined as mRS ≤1 was significantly increased at 6 months and persisted up to 18 months after a stroke. © 2015 S. Karger AG, Basel. en_US
dc.language.iso en_US en_US
dc.publisher Karger Publisher en_US
dc.subject NeuroAiD Efficacy en_US
dc.title Chinese medicine NeuroAiD efficacy on stroke recovery - extension study (CHIMES-E): A multicenter study of long-term efficacy en_US
dc.type Article en_US


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