Suggestions(5)
Exact(3)
The relationship between the study arm and the total of intervention and patient health care costs was also analyzed.
There were no statistically significant (P>0.05) associations between any of the pretreatment patient characteristics as reported in Table 1 and clinical trial entry, nor was there any statistically significant interaction between the study arm and these characteristics.
A sample size of 37 would achieve at least 80% power to detect a PFS difference of 4 weeks between the study arm and historical control data at a two-sided 0.1 significance level (type I error).
Similar(57)
Data concerning the rate of crossover between the study arms were also collected.
However, there were differences between the study arms in the level of support provided by researchers for the delivery of FootyFirst.
Rates of any bleeding and major bleeding were similar between the study arms in both RE-COVER (Figure 2B) and RE-COVER II [20, 21].
Mixed models repeated measures analysis revealed significant differences between the study arms regarding total PANSS score change favouring n-3 PUFA (p = 0.016; effect size (ES) = 0.29).
Efficacy and safety will be compared between the study arms and in patient subgroups including patients with nonsquamous versus squamous tumor histology and patients who received prior bevacizumab treatment.
Measured baseline characteristics did not differ significantly between the study arms.
For randomization of the ZAMSTAR study, we determined the balance between the study arms using each method.
Reasons for withdrawal from the study are shown in Figure 1; there were no apparent differences between the study arms for adults or children.
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