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1 ven approaches wherein a circuit of interest is defined a priori.
2 , 279 (37.5%) were in a high-risk group that was defined a priori.
3 ere were 21 reported secondary outcomes that were defined a priori.
4 e date for the paired controls; time windows were defined a priori.
5 motor, diplopia, and HRQOL criteria, success was defined a priori and applied separately and in combi
6 Cutoffs for deranged physiologic parameters were defined a priori and their association with in-hosp
15 ale (HAM-A) and Visual Analog Scale for Pain were defined a priori as key secondary outcome measures.
16 samorelin, those with >/=8% reduction in VAT were defined a priori as responders per the statistical
19 subgroups should be few in number and should be defined a priori on the basis of variables present be
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