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Clinical Trial Summary

The purpose of this study is to estimate the incidence and severity of peristomal skin lesions and evaluate the progression of the peristomal skin condition at 8-15 days following application of the barrier.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01526967
Study type Observational
Source ConvaTec Inc.
Contact
Status Unknown status
Phase N/A
Start date January 2012
Completion date December 2012

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