Clinical Trial

A Proof-of-Concept Study to Evaluate the Efficacy of NOBO, a Novel Postbiotic, in Controlling Axillary Odor in Healthy Adults

Completed
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Summary
The goal of this clinical trial is to evaluate the performance of NOBO, a yeast-based fermentation product (postbiotic) designed to control axillary odor, in controlling axillary odor in healthy male and female adults age 18 - 70 with confirmed self-perception of body odor. The main question it aims to answer is: Does NOBO decrease self-perceived odor of the intervention axilla compared to the placebo axilla at any time point? Researchers will compare the intervention axilla to the placebo axilla to see if there is a difference in self-perceived odor and microbiome. Participants will: * be given a NOBO deodorant spray and a placebo deodorant spray (each assigned to one axilla) * self assess body odor * sample axilla with cotton round for 3rd party odor assessment * sample axilla with a swab for skin microbiome analysis via qPCR * self assess skin irritation
Protocol Amendment History 2 changes
critical Trial completed 2026-05-12
critical Primary endpoint(s) modified 2026-04-28
Trial Details
NCT Number NCT07547761
Lead Sponsor Kingdom
Conditions Body Odor
Enrollment 5 participants
Start Date 2026-04-16
Primary Completion 2026-05-04 (estimated)
Study Completion 2026-05-04 (estimated)
Updated on ClinicalTrials.gov 2026-05-11