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Clinical Trial Summary

The purpose of this study was to compare two wound dressing products for partial thickness burns in adults.


Clinical Trial Description

After being informed about the study, all patients that had given written informed consent underwent screening. If eligible study participants were randomized to be treated wih either the standard dressing of care; pigskin or a microbial cellulose. Dressing were applied within 72 hours after burn injury. Evaluation was done in an open manner due to the specific characteristics of the dressings. Study particpants were followed weekly until complete wound closure and after that evaluated at 6 and 12 months after injruy for burn scar outcome. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04412759
Study type Interventional
Source University Hospital, Linkoeping
Contact
Status Completed
Phase N/A
Start date June 2016
Completion date November 2019

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