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Continuous variables (baseline homocysteine levels, trial proportion with diabetes, trial proportion with cardiac disease, average follow-up time, and number of events in the study) were also explored using metaregression in sensitivity analyses, with results confirming that none of these factors had a significant impact on the overall meta-analysis (results not shown).
Secondary outcomes were helpfulness of the HHF and the wristband after two months, change of breathlessness severity between baseline and month two, and uptake into the trial (proportion of patients from the longitudinal study participating in the RCT).
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In the first trial, proportions of damaged sperm cells in each sample determined by the automated procedure agreed closely (r2 = 0.98, P < 0.001) with the predicted theoretical values.
Median values were obtained for each characteristic per arm when applicable, and overall trial proportions were calculated from data provided in the trial's study characteristics.
Table 5 The comparative subjective quality evaluation results Number of observers Comparison clips for each observer Total number of scoring trials Comparison scale Number of scoring trials Proportion Statistical mean 95% confidence interval for statistical mean (α = 0.05) 50 90 4500 0 4478 99.51 % 0.005[0.0030, 0.0070] 1 22 0.49%.
We used a modified version of the threshold estimation procedure described by Levitt Levittt, 1971), changing mask contrast according to participant's 'Seen' trials proportion in a block.
To provide indices of eWMC for each trial size, proportion of trials correct for the neutral trials were subtracted from proportion correct for the emotional trials.
Similarly to the BoTULS trial the proportion of patients achieving their principal active functional goal with onabotulinumtoxinA plus standard of care was not statistically different from placebo plus standard of care.
We tested an approach that combines into a single statistic, the drug effect in those who complete trial and proportion of patients in each treatment group who complete trial.
In the EPHT Trial, the proportion of women with vasomotor symptoms was higher (Table 2).
In the present trial, the proportion of dead worms analyzed in the available nodules after doxycycline was 54% (PP).
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