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Clinical Trial Summary

The goal of this study is to evaluate the impact of Customizable in the management of extensive closed surgical incisions for Subjects undergoing abdominal surgery for incisional hernia repair and/or functional panniculectomy as compared to SOC dressing, and to significantly reduce the SSC rate experienced by Subjects receiving Customizable vs. SOC surgical incision dressing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02302222
Study type Interventional
Source 3M
Contact
Status Terminated
Phase N/A
Start date May 2015
Completion date July 31, 2017

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