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Clinical Trial Summary

The objective of this study is simulate the clinical use of an antiseptic solution in a 24 hour window and the recovery to baseline conditions at 1 month following application. Efficacy will be simulated as the capacity of the material to reduce or clear the skin bacterial population from a representative skin area: the anteromedial forearm.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05608382
Study type Interventional
Source Center for Innovation and Research Organization
Contact
Status Completed
Phase N/A
Start date March 7, 2022
Completion date March 18, 2022

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