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The primary pain regulatory measure for which the study was powered is temporal summation (TS), which approximates ascending pain facilitation.
The study was powered a priori, for the primary endpoint.
The study was powered to detect a 40% reduction in relative risk of POAF.
The study was powered to show a possible difference for the primary endpoint.
With this sample, the study was powered to detect a 35% difference under the same circumstances.
The study was powered to detect an increase in intrarenal pressure.
This study was powered to find an association of at least r=0.5 to be statistically significant.
This study was powered to detect a difference in a clinical score not rates of hospitalization [2].
The study was powered for the primary analysis.
The study was powered to detect a 36% reduction in mortality at 18 months.
The study was powered to detect a 30% reduction in the mean longitudinal diarrhoea between the two groups.
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