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Clinical Trial Summary

This single site study is a randomized, controlled, partially-blinded design enrolling a minimum of 516 healthy volunteers, where each subject will receive two of the planned study products on the product application sites of the abdomen and/or groin.


Clinical Trial Description

To demonstrate the antimicrobial activity of the Investigational Product (IP) by comparing counts of resident skin microbes, obtained after IP application to intact skin of the abdomen and groin, to counts obtained prior to application. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04035161
Study type Interventional
Source Becton, Dickinson and Company
Contact
Status Completed
Phase
Start date April 17, 2019
Completion date December 24, 2019

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