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  • Celkem 42,2% pacientů ze skupiny kandesartanu (95% CI: 39,5 až 45,0) a celkem 46,1% pacientů ze skupiny placeba (95% CI: 43,4 až 48,9) dosáhlo tohoto koncového parametru, absolutní rozdíl činil 3,9% (95% CI: 7,8 až 0,1). (cs)
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