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Areas with stents at baseline were not evaluated.
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Baseline to week 28 and baseline to week 52 changes were not evaluated separately as the week-by-treatment interaction effects were not statistically significant.
Additionally, potential confounders, e.g., history of peripheral vascular disease and serum lipid levels, were not evaluated at baseline.
Post hoc multivariate Cox regression models showed that baseline EQ-5D index values (VAS scores were not evaluated) were not significantly associated with time to achieving the composite endpoint proposed by Zinman et al. [ 33].
It is possible that there were inherent differences between the groups that were not evaluated or adjusted at baseline.
Mice that were not infected with P. gingivalis were not evaluated weekly, but only at baseline and sacrifice.
Second, study-specific covariates (i.e., baseline comorbidities, stage and duration of disease, variations by geographic region and publication year) were not evaluated.
Correlations with changes in IFN-γ levels were not evaluated because of the small number of patients who had detectable IFN-γ levels at baseline.
Placebo comparators were not evaluated.
Earlier time points were not evaluated.
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