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PORCINE XENOGRAFT OR MICROBIAL CELLULOSE IN THE TREATMENT OF PARTIAL THICKNESS BURNS - A RANDOMISED CLINICAL TRIAL
The purpose of this study was to compare two wound dressing products for partial thickness burns in adults.
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
The Burn Centre at Linköping University Hospital,
Linköping, Sweden
Start Date
June 1, 2016
Primary Completion Date
November 1, 2018
Completion Date
November 1, 2019
Last Updated
June 2, 2020
26
ACTUAL participants
microbial cellulose
OTHER
Lead Sponsor
University Hospital, Linkoeping
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07277166