Evaluation of the Antimicrobial Effectiveness of CHG/IPA

Status Completed

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

Clinical Trial Details

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

View Details

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