Keloid Clinical Trial
Official title:
Influence of a Silicone Gel (Dermatix®) on Thoracic Scar Formation After Harvesting of Autologous Rib Cartilage for Standardised Total Ear Reconstruction
So far the evaluation of scar treatment was based on subjective criteria. The patient groups
were divided into treated versus non-treated.
In this study we use patients undergoing ear reconstruction with autologous rib cartilage.
The thoracic scar of harvesting the rib cartilage is routinely reopened after 3 month during
second stage of reconstruction. Therefore we have a ideal model of clinical, physiological
and histological scar evaluation in a homologous patient group.
All patients randomly treat one half of the scar with a silicone gel (Dermatix). The other
half is untreated as an internal control.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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