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ispitanici su bili randomizirani u omjeru 1:1 u skupine koje su primale salmeterol/fp 50/250 (ukupni itt n=776) ili salmeterol (ukupni itt n=778).
subjects were randomised 1:1 to salmeterol/fp 50/250 (total itt n=776) or salmeterol (total itt n=778).