Clinical Trial

Examine Impact of Topical Application of Active Versus Placebo on the Skin Microbiome in Sensitive Skin.

Study acronym: SkinBiome
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Record status
This record was last updated March 6, 2026 (before its estimated April 2026 completion). Its status may not reflect the trial's current state.
Summary
The purpose of this study is to build insights to understand how the placebo and active impacts the skin microbiome in women with high skin sensitivity (SS10 \> 13) and sun exposure. Microbiome samples will be taken at baseline after 2 weeks of using the placebo (base without active) as a run-in period followed by the usage of placebo for an additional 4 weeks. The participants will then start the usage of active formula for an additional 8 weeks with microbiome samples collected at the 10-week and 14-week. This will allow us to observe how the microbiome changes over time after the product usage of both placebo and active formulations relative to the pre-regimen condition. In addition, headshot photos will be taken using the Haut AI application at each time point concurrent to the microbiome sample collection to examine changes in skin appearances after the regimen.
Trial Details
NCT Number NCT07454525
Lead Sponsor AB Biotics, SA
Collaborators: Hellobiome, Kaneka Americas Holding Inc.
Conditions Skin, Skin Microbiome, Skin Microbiota, Skin Ageing
Enrollment 45 participants
Start Date 2026-02
Primary Completion 2026-04 (estimated)
Study Completion 2026-06 (estimated)
Updated on ClinicalTrials.gov 2026-03-06