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Clinical Trial Summary

This study aims to assess the efficacy of a custom fitted device designed to isolate enteroatmospheric fistulas effluent independent of negative pressure wound therapy and to evaluate the effects on the device related to dressing changes, time required for dressing changes, management costs, and the ease of use.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04978090
Study type Interventional
Source University of Kentucky
Contact
Status Completed
Phase N/A
Start date July 1, 2021
Completion date September 16, 2022

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