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Clinical Trial Summary

The purpose of this study is to demonstrate substantial equivalence in terms of safety to support an indication change related to the usage of Prevena Therapy for up to 14 days. The enrolled subject will undergo 1 of 4 surgery types and be evaluated for up to 90 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05614869
Study type Interventional
Source 3M
Contact Eric Synatschk, MS, CCRP
Phone 346-550-5698
Email esynatschk@solventum.com
Status Recruiting
Phase N/A
Start date February 2, 2023
Completion date May 25, 2027

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