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These parameters were assessed on 15 areas of the body.
Several clinical outcome parameters were assessed.
In each case, the pore parameters were assessed.
Examination quality was documented and safety parameters were assessed.
Somatic parameters were assessed through standardised medical records.
Safety parameters were assessed at baseline and at 2 weeks, 2 months (visit 5) and 4 months (visit 9, end of the study) following randomization.
Using the Pearson correlation method, the correlations among evaluated parameters were assessed.
Four damage indicators based on modal parameters were assessed by comparing pristine and damaged states.
Consolidation parameters were assessed by statistical analysis of the oedometer test data.
Safety parameters were assessed in all women who were treated with the study drug.
Composition, texture parameters, colour, lipid oxidation, microbiological and sensorial parameters were assessed.
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