SCARWARS study deals with the first on-human evaluation of a compressive device dedicated to the prevention of keloïd scars recurrence after surgery. The tested device is made with clinical grade silicon. SCARWARS is a monocentric study. 27 patients will be include and follow during one year. The primary outcome of this study is the number of keloid recurrence after treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
31
interventions on patient are : * surgical excision of ear lobe keloid * application of compression device on sutured skin
CHU de Besançon
Besançon, France
Recurrence of keloid scar
Recurrence will be assessed during each visit by surgeon
Time frame: 12 month
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