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Of these 141 NI trials, we identified 35 post-authorization trials.
Only three of the trials we identified were at low risk of bias.
From this composite of clinical trials, we identified several factors that modulated the magnitude of the vibriocidal antibody response.
From the 36 trials we identified 14 that reported, either directly or indirectly, the mean age and standard deviation of the treatment groups.
As haemoglobin values were collected sequentially over time in both trials, we identified an opportunity to evaluate changes in haemoglobin values in these two independent trials.
Rates of adherence to thiazide therapy ranged from 67%to87%7% in the randomized controlled trials we identified reporting such rates [ 20- 24].
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A possible and anticipated weakness may be the quantity and quality of the trials we identify.
A possible weakness may be the quality of the trials we identify.
Based on the data from an international thromboprophylaxis trial, we identified risk factors other than APACHE II score which predicted 60-day hospital mortality and 60-day ICU mortality.
By means of the above-mentioned statistical analysis of the first trial, we identified several points to be improved: a) there was a considerable number of outliers.
For each trial we identified a peak value in the skin conductance response (SCR) within 1 4 s of the onset of the threat stimuli.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com