Efficacy and safety of mildronate for acute ischemic stroke: A randomized, double-blind, active-controlled phase II multicenter trial

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Abstract

Background and Objective: Mildronate, an inhibitor of carnitine-dependent metabolism, is considered to be an anti-ischemic drug. This study is designed to evaluate the efficacy and safety of mildronate injection in treating acute ischemic stroke. Methods: We performed a randomized, double-blind, multicenter clinical study of mildronate injection for treating acute cerebral infarction. 113 patients in the experimental group received mildronate injection, and 114 patients in the active-control group received cinepazide injection. In addition, both groups were given aspirin as a basic treatment. Modified Rankin Scale (mRS) score was performed at 2 weeks and 3 months after treatment. National Institutes of Health Stroke Scale (NIHSS) score and Barthel Index (BI) score were performed at 2 weeks after treatment, and then vital signs and adverse events were evaluated. Results: A total of 227 patients were randomized to treatment (n = 113, mildronate; n = 114, active-control). After 3 months, there was no significant difference for the primary endpoint between groups categorized in terms of mRS scores of 0-1 and 0-2 (p = 0.52 and p = 0.07, respectively). There were also no significant differences for the secondary endpoint between groups categorized in terms of NIHSS scores of >5 and >8 (p = 0.98 and p = 0.97, respectively) or BI scores of >75 and >95 (p = 0.49 and p = 0.47, respectively) at 15 days. The incidence of serious adverse events was similar between the two groups. Conclusion: Mildronate injection is as effective and safe as cinepazide injection in treating acute cerebral infarction. © 2013 Springer International Publishing Switzerland.

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Zhu, Y., Zhang, G., Zhao, J., Li, D., Yan, X., Liu, J., … Zhao, G. (2013). Efficacy and safety of mildronate for acute ischemic stroke: A randomized, double-blind, active-controlled phase II multicenter trial. Clinical Drug Investigation, 33(10), 755–760. https://doi.org/10.1007/s40261-013-0121-x

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