A 12-Week Randomized, Double-Blind, Placebo-Controlled Trial for the Efficacy and Safety of a Novel Nutraceutical for Mild-to-Moderate Acne

Background

Acne is a common skin issue that many people face. There are various treatments available, but recent studies suggest that inflammation in the body may also play a role in acne. Some natural supplements, including plant-based products, may help address these underlying causes. However, there are not many well-conducted studies to confirm their safety and effectiveness.

Aims

This study aimed to evaluate how safe and effective a new oral supplement is for women with mild to moderate acne.

Methods

In this 12-week study, 102 women participated. They were divided into two groups: one group received the active supplement, while the other received a placebo (a non-active treatment). All participants followed the same skincare routine. The main goal was to see how much their acne severity improved after 12 weeks.

Results

Out of the 102 women, 92 completed the study. Those taking the active supplement showed significant improvements in their acne severity compared to those on the placebo. More women in the supplement group reported clearer skin, and there were notable reductions in both types of acne lesions. Overall, skin health improved significantly for those taking the supplement.

Conclusion

The oral supplement was found to significantly improve mild to moderate acne and enhance overall skin health in adult women compared to a placebo.

Opportunities for Clinics and Patients

Based on the trial data, clinics can set clear goals for treating acne with this new nutraceutical. Measurable outcomes include improvements in acne severity and overall skin health.

AI Tools for Clinical Needs

Clinics can select AI solutions that fit their specific needs to enhance patient care and track treatment effectiveness.

Implementation Steps

Start with a pilot project using the new supplement, monitor results, and assess the real-world impact of the treatment.

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