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Patients just after anesthesia induction were randomized, allocated in two groups: one receiving corlopam at the dosage of 0.05 μg/kg per min (Group A) and the other receiving placebo (Group B).
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Studies were included if randomized, allocating one or more groups to statin therapy and reporting dichotomous outcomes relevant to the assessment of CIN.
Calves were weighed (avg. 133.0 kg), randomized, and allocated to one of the three treatments.
All participants were randomized and allocated to intervention.
Participants were then immediately randomized and allocated to one of the two interventions.
Between August 2010 and August 2012, 173 children were randomized (86 allocated to q.d., 87 to b.i.d).
The care managers will be randomized and allocated to the intervention (CSC) or the control group (CAU).
Of these, 343 met the inclusion criteria, and were therefore invited to participate in the study, see figure 1. See figure 1 for number of persons randomized, receiving allocated intervention, having baseline data and reasons for not participating.
After informed consent is provided and baseline assessment (T0) has taken place, participants will be randomized and allocated to either CAU + SOS training or continue to receive CAU. Follow-up assessments will take place 2, 8 and 14 months after baseline assessment.
Patients were randomized by allocating patients with an odd number to the group for LON and patients with an even number in the conventional method group.
Of 349 eligible patients, 177 were randomized: 89 were allocated hysterectomy and 88 were allocated UAE.
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