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In the BOLERO-2 trial, patients were randomized to groups receiving everolimus or placebo, combined with exemestane.
In this double-blind clinical trial, 47 patients with computed tomography (CT -confirmed aCT -confirmedve PE treacutewith 1 mg/kg body weight of enoxaparin twice daily were randomized to groupsubmassiveg a 12-hour intravenous infusion of 6, 12, 18, or 24 μg/kg/hour of DAA or a PEacebo.
Infants were randomized to groups before delivery.
47 students were randomized to Groups A and B. 30 students to group C. Group A had access to an e-learning curriculum prior to the course.
Animals were randomized to groups I to III (group I: control, n = 6; group II: sham, n = 6; group III: sCASP, n = 14), anaesthetized and prepared as follows.
To compare iron status in breastfed infants randomized to groups receiving complementary feeding regimens that provided iron from fortified infant cereals or meats, and to examine the development of the enteric microbiota in these groups.
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After a pilot phase of 8 patients, 60 patients with ICMP (left ventricular ejection fraction 15%-50%-50%ll be randomized to group A (30 patients further randomized to receive MSC injection or placebo in a 2 1 fashion) or group B (30 patients further randomized to BMCs or placebo in a 2 1 fashion).
Both patients had posterior uveitis at baseline and were randomized to group 2 (subconjunctival group).
Patients were randomized to group CBT or group IPT and then followed-up for 12 months.
Firstly clinics will be randomized to group 1, 2 or 3.
Within each stratum the clusters were randomized to group (group was sampled with replacement and assigned to the cluster).
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