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The intergroup comparisons also mirrored the primary analysis, with no significant contrasts at ARDS diagnosis, but clear contrast after 24 h (group IV vs. group I and II) (Additional file 1: Table E3).
To gather more non-ambiguous results, a primary analysis with an experimental design is preferred.
Repeating the primary analysis with a fixed effects model confirmed the overall results (relative risk 1.75, 1.59 to 1.92).
We did the primary analysis with an independent samples t test with birth weight as the primary outcome.
This analysis retains the conclusions from the original primary analysis with effects that point in the same direction.
The primary analysis (with adjustment for site and baseline body weight) showed a group difference in weight loss of 2.70 kg (95% confidence interval 1.70 to 3.67 kg).
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We repeated the primary analysis with re-categorization of patients according to the RRT modality received for the majority of treatment sessions during the first 30 days.
SCF and JK were responsible for the primary analysis, in consultation with RRH.
Provides the results of the primary analysis of SeMaS with the criterion measures and PAM-13.
In primary analysis, subjects with missing data were excluded, but in sensitivity analyses, patients with missing data were included with imputation of missing information [ 16].
The primary analysis is with completers.
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