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Those who have improved substantially (defined as being afebrile, and having a lower cellulitis severity score) will be randomized at day 6 between additional 6 days of oral flucloxacillin (n = 198) or placebo (n = 198).
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For the in vivo assessment of viral protein expression and replication, shown in Fig 8 and 9 (panels D and E), animals were randomized at day 0 into two groups (n = 3) and treated by intratumoural injection of 2.4 × 10 H-1PV virus genome (Vg)/animal with or without intraperitoneal administration of VPA (100 mg/kg/d).
In a prospective, multicenter, open-label study, de novo liver transplant patients were randomized at day 30±5 to (i) everolimus initiation with tacrolimus elimination (TAC Elimination) (ii) everolimus initiation with reduced-exposure tacrolimus (EVR+Reduced TAC) or (iii) standard-exposure tacrolimus (TAC Control).
All the array experiments were performed simultaneously at the same day, and PD and control samples were randomized at each BeadChip, ruling out any potential batch effect.
In (d), all three parameters are randomized at the same time.
Subjects were randomized at the completion of all baseline assessments.
Two hundred seventeen patients were randomized at 4 bariatric centers in Switzerland.
Adherent, eligible enrollees were randomized at the baseline visit.
The order of testing was randomized at each interval.
Thus, pathogen genotype was randomized at the whole-pot level, while host genotype was randomized at the split-pot level.
One cluster RCT was randomized at clinic [ 18], and the remaining four trials were randomized at a patient level [ 14- 17].
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