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In such trials, participants agree to receive either a sirolimus-coated stent or a standard stent.
In such trials, scientists randomly assign patients to treatment or control groups with the aim of eliminating bias from clinician and patient decisions.
In such trials, statistical power is governed by the rate of disease events in each group and cost is determined by randomization, treatment, and follow-up.
In such trials, groups of similar patients undergo either a new form of treatment, the standard treatment of the time or a placebo treatment.
In such trials, judgment on the incremental value of patient reported outcomes would have been highly hypothetical.
In such trials participants make an error centred on the orientation of other (non-probed ) items in memory (Fig. 2C).
In such trials, patients are randomised to either receive the standard chemotherapy treatment or a biomarker-directed treatment arm, in which biomarker status is used to guide treatment.
In such trials, clinical relevance would refer to the added benefit claims of a specific drug, apart from efficacy, relative to its comparator drug in the trial.
In such trials, both the efficacy of adjusted treatment in normalizing response and the effect of inaccuracies of prediction will be combined.
In such trials, eligible patients are asked whether they have a preference for one of the two (or more) treatments and whether they agree to be randomized.
In such trials patients are preferably referred in a regular manner to treatment and extensive exclusion criteria should not be used.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com