??? ??? ????? ?????? ??? ???? ?????? ?????? ??????. ??? ????? ?????? ?????? ????? ??? ???? ?????? ?????? ?????? ??? ????? ?????.If a statistical test within Each individual pairwise comparison was important for that higher dose comparison on the nominal 0.05 level, two-sided (in favor of the tramadol arm) for the 1st endpoint, then testing was to c
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7% study completion rate) have been able to tolerate the study medication effectively. The tramadol twenty five mg was identified not to be statistically noticeably distinct from placebo in the key Evaluation (SPID48), and so formal testing of the key secondary conclusions was not done for tramadol twenty five mg, in accordance with the predefine