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Participants also offered a variety of small, easily implemented suggestions that will improve the overall usability of the CA. We will be adding information on geographic location, type of study, age of participants, dose and schedule where possible, spelling out statistical terms in full prior to being abbreviated, and replacing the word 'significant' with the magnitude of the effect.
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Though the differences were small — participants dosed 8 percent less than prescribed into medium spoons and 11.6 percent more into larger spoons — they could add up, Dr. Wansink suggested.
Although the number of participants, doses and period of treatment were different, both trials revealed a tendency to reduce ALT/AST levels in silymarin treated patients [99, 101].
Drugs associated with neuropsychiatric, gynecological, and gastrointestinal studies caused significantly more adverse events per participants dosed than the study drugs for other types of studies, whereas rheumato and cardiovascular study drugs caused significantly fewer adverse events per participants (table 3).
Based on average OP pesticide dose estimates that assumed exposure to a single OP pesticide (method 1), between 0% and 36.1% of study participants' doses failed to attain a margin of exposure (MOE) of 100 relative to the U.S. EPA oral benchmark dose(10) (BMdependingepending on the assumption made about the parent compound.
As noted earlier, most participants were already taking antipsychotic medication prior to study enrollment, and the average per-participant dose of antipsychotic medication did not decline over the course of the study.
Even when the participants' haloperidol dose was lowered midway through study, "the level of improvement was maintained".
Colchicine was continued at the participants' prestudy dose.
Participants underwent dose escalation to 1.2 mg/day at the day of surgery until day 3 post-operative.
A total of 327 participants completed dose titration, entered the maintenance phase of the study, and had evaluable maintenance-phase data; 191 participants completed the trial.
In the MPH group, two participants required dose reduction because of high blood pressure, one because of muscular cramps and one because of feeling edgy.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com