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For instance, the first trial of subject 1 initiated 90.765 s after the experiment started.
Figure 12(b) displays the estimation and measurement of pronation/supination angle for a trial of subject 2. In this figure, we observe that there is an underestimation of the angle.
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We analyzed the effects of baseline symptom severity and placebo response magnitude on the decision to dose escalate in a 12-week, randomized, double-blind, flexible dose antimuscarinic trial of subjects with overactive bladder symptoms.
Of the clinical trials, the JUPITER trial of subjects with elevated high-sensitivity C-reactive protein (hsCRP) levels demonstrated how a biomarker can be used clinically to identify persons who might benefit from aggressive statin therapy [ 3].
54, 55 The PRESTO study (Parkinson's Rasagiline: Efficacy and Safety in the Treatment of "Off") was a randomized, placebo-controlled, double-blind trial of subjects with advanced PD with motor fluctuations.
Trials included in this review were dual-therapy trials of subjects who were already taking background metformin and were assigned to receive canagliflozin, glimepiride, or sitagliptin.
For trials of subjects who suffered stroke, gait speed was calculated after experiments, to observe how it was affected under the use of our vibrotactile device.
The grip force trajectory of each individual trial of each subject was first normalised against the maximal force each subject achieved in the V condition.
The grip force trajectory of each individual trial of each subject was normalized against the average maximal force that the subject achieved in their maximal effort trials.
Values were obtained from the first MVC trial of each subject.
For example, in a modeled trial of 500 subjects, misallocation of CCL3L1-CCR5 genofype onlynly 25 (5%) subjects between placebo and vaccine arms results in a relative error of ∼12% from the true vaccine efficacy.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com