The purpose of this study is to assess the efficacy of autologous epidermal cells suspension grafting using a newly developed device named VITICELL® compared to placebo. The secondary objective is to evaluate safety of VITICELL® and global satisfaction of patient and investigator.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
38
Department of Dermatology - Ghent University Hospital
Ghent, Belgium
University Hospital Center of Bordeaux
Bordeaux, France
CHU Le Mans
Le Mans, France
Dr Michel PASCAL
Paris, France
San Gallicano Dermatological Institute
Rate of successful repigmentation
succesful repigementation define as more than or equal to 50% repigmentation of the treated area
Time frame: at month 6
Rate of successful repigmentation
succesful repigementation define as more than or equal to 50% repigmentation of the treated area
Time frame: at month 12
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Roma, Italy