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They were randomized into group A or B, each consisted of half of the total study population.
Interventions: Patients were randomized into group C (centrifugal pump for cardiopulmonary bypass; n = 54) and group R (roller pump for cardiopulmonary bypass; n = 49).
The randomization was performed in two separate groups for GTs 1/4 and for GTs 2/3. 2 male patients, both randomized into group A, withdrew their consent before the first application of study medication.
87 patients enrolled in the trial were randomized into group I (n = 24), II (n = 32) and III (n = 31).
After recruitment, subjects signed consent forms, completed background questionnaires, and were randomized into group A or group B matched by gender, age, and baseline HbA1c.
One hundred and twenty-three patients (78 males, 45 females, median age 62.7 and 60 years, respectively) were randomized into group A (SOFA 19.27) and group B (SOFA 10.23).
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They were ranked on pretest accuracy and then randomized into groups.
Once tumors were established (100 to 200 mice, mice were randomized into groups with similar mean tumor volumes at the start of the study.
Once tumors were established (150 200 mice, mice were randomized into groups with similar mean tumor volumes at the start of the study.
When tumors reached an average volume of about 100 mm3 (50∼200 mm3), the animals were randomized into groups.
After 10 days of acclimation, the 40 rats were randomized into groups of 10.
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