Suggestions(4)
Exact(1)
Although there were no apparent clinically significant differences between treatment and control groups in the number of tumour progressions in individual trials, rate of tumour progression was lower with epoetin beta than control in the meta-analysis (0.62 vs 0.81 events/patient-year) (Table 3).
Similar(58)
In a 64-channel EEG study using electrical stimulation at the threshold level, trials perceived as painful were characterized by a lower prestimulus theta connectivity, compared with trials rated as nonpainful [67].
When contrasting only trials rated for pain intensity, the effect for the right insular ROI was significant (F 1,16) = 6.34, P = 0.023) – being related to reduced activation during biopsies on the numbed hand evaluated for pain intensity (Figure 7).
Proportion of trials rated as replicable (primary outcome).
Trials rated as 3 and 4 were considered "uncertain".
Five trials rated pain relief in addition to pain intensity.
36 In the major DRV trials, rates of side effects were generally low.
Proportion of trials rated as having a complete description of the intervention (primary outcome measure).
For all of the analyses, trials rated with a confidence level of 1 or 2 were considered to be "undetected" partial errors whereas trials rated with a confidence level of 5 or 6 were considered to be "detected" partial errors.
We also did sensitivity analyses for those outcomes including additional trials rated as at high risk of bias.
43 44 No valid method exists for combining the results of trials rated as high risk and low risk of bias.
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