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In the primary analysis, a participant was censored at the last study visit date if vital status at 12 weeks was unknown (i.e., lost to follow-up).
For the primary analysis a covariance analysis (ANCOVA) will be conducted.
After the primary analysis, a subgroup analysis was performed according to gender and discipline.
Second, in the primary analysis a cut-off point for compliance of 85% was used.
After the primary analysis, a subgroup analysis was performed according to gender.
In the primary analysis, a statistically significant PFS benefit was observed in the panitumumab + FOLFIRI versus FOLFIRI group (Table 3).
Similar(29)
In the primary analysis, an improved response rate and PFS were observed, but with an imbalance of toxicity in the cediranib arm compared with the control arm.
The primary analysis (labeled A) used a proportional odds model to estimate the odds of more elevated (>75th percentile) biomarkers.
This test presupposes that a primary meta-analytic result can be identified in each systematic review (analogous to a primary analysis in a clinical trial).
To gather more non-ambiguous results, a primary analysis with an experimental design is preferred.
main baseline covariates, will be considered as a mandatory part of the primary analysis and a proper interpretation of efficacy.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com