Abstract
The randomized clinical trial has been applied in cerebral vascular disorders for nearly 30 years. The amount of research coming from Canada and the United States in the field of stroke prevention by biological agents and drugs is appropriate because of historical events. For example, heparin emerged from the laboratories of Dr. Charles Best at the University of Toronto [1], and Dr. Hugh Smythe working in Dr. Fraser Mustard’s laboratory at the same institution was the first to detect the platelet-inhibiting properties of any potentially therapeutic compound, sulfinpyrazone [2]. Within a year, Dr. Harvey Weiss in New York described the platelet-inhibiting action of aspirin [3]. It is somewhat artificial to divide the work of North Americans from that of Europeans in any field because of the cross-fertilization of ideas and collaborative studies. The first platelet-inhibiting drug to be put to the test of a clinical trial was dipyridamole. Its mode of action as a platelet antagonist was defined by a Canadian, Dr. Patricia Emmons, working in the Department of Hematology in Oxford [4].
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Barnett, H.J.M., Meldrum, H., Eliasziw, M. (2001). Clinical Trials in Stroke Prevention in North America. In: Guiloff, R.J. (eds) Clinical Trials in Neurology. Springer, London. https://doi.org/10.1007/978-1-4471-3787-0_18
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DOI: https://doi.org/10.1007/978-1-4471-3787-0_18
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