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Clinical Trial Summary

This prospective, multicenter, single-arm observational study aims to document the clinical performance and safety of a sterile, bacteria-binding, super-absorbent wound dressing for the intended use in a daily clinical practice. 50 patients (male/female) with superficial wounds of any etiology affecting only epidermis and dermis layer, with one or more clinical signs of infection or at high risk of infection and also high to very high exudate levels will be observed over a period of 14 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02662218
Study type Observational
Source BSN Medical GmbH
Contact
Status Completed
Phase N/A
Start date July 2016
Completion date February 2017

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