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. 2017 Apr 24;48(5):1262–1270. doi: 10.1161/STROKEAHA.116.014321

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© 2017 The Authors.

Stroke is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.

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Figure 1. — Patient flow diagram. The numbers presented are as treated. There were 2 patients who were randomized to the placebo group but received an incorrect kit, which after unblinding was determined to have contained Actovegin. Those patients are included as randomized for the intent-to-treat (ITT) analyses (placebo group) and as treated for the safety analyses (Actovegin group). More than 1 reason for discontinuation could have been selected.