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The primary objective of this investigation is to evaluate if complications related to surgical wound are more common in the treatment group compared to the control group starting from operation day u...
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Lead Sponsor
Molnlycke Health Care AB
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University Hospital Gent, Belgium
Ghent
Medisch Centrum Latem
Sint-Martens-Latem
Södersjukhuset
Stockholm
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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