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Clinical Trial Summary

This single-center, open, non-randomized study aims the efficacy evaluation of Effaclar Duo+M and Effaclar+M Purifying foaming gel on total acne lesion count, pigmented lesions and scars for 6 months in subjects with mild to moderate facial and truncal acne.


Clinical Trial Description

The study will be conducted in accordance with the principles of Resolution 466/2012 of the Conselho Nacional de Saúde do Brasil3, ethical principles from the Declaration of Helsinki (and subsequent modifications) and Good Clinical Practice. Statistical methodology: Quantitative variables, or those that can reasonably be treated as such, are summarized using the minimum, maximum, measures of central tendency such as the mean and median & measures of dispersion such as the standard deviation (SD). Qualitative variables are summarized in the form of counts and percentages. Significance level: The null hypothesis will generally be rejected if a p-value less than 0.05 (5% significance level) is produced by the statistical procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06463925
Study type Interventional
Source Cosmetique Active International
Contact Alessandro Nascimento
Phone +55 21 98726-2046
Email a.nascimento@cidp-cro.com
Status Recruiting
Phase N/A
Start date December 7, 2023
Completion date September 2024

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