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A portable whole body bioimpedance spectroscopy device (BCM Fresenius Medical Care D GmbH) will be used for BIA measurement at baseline for both arms of the study.
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Patients who developed any of the outcome events within 1 year after the baseline were also excluded for both arms.
This practice increased by 20% from baseline in both arms.
Baseline characteristics of women will be summarised for both arms of the trial.
We will use descriptive statistics to assess balance between the trial arms at baseline for both clinic and individual participant characteristics.
For outcomes which failed the normality test (e.g. BODE score), Wilcoxon signed ranks test is applied to compare week 26 (week 14/ week 2) to baseline for the two arms, respectively.
For normally distributed outcomes (e.g. CCQ and SGRQ scores), paired t-test was applied to compare week 26 (week 14/ week 2) to baseline for the two arms, respectively.
Mean plasma viral load was 4.9 and 4.8 log10 copies/ml at baseline for the MVC and EFV arms, respectively.
Repeat for both arms.
The baseline for both handsets is impressive.
We compared the differences in the distribution of patients among the eight possible model HS (HS with undetectable VL are not possible at baseline) for the LPV/r arm and the efavirenz (EFV) arm using a Chi square test (Table 4).
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