Clinical Trials Directory

Trials / Unknown

UnknownNCT00565552

Influence of a Silicone Gel (Dermatix®) on Thoracic Scar Formation After Harvesting of Autologous Rib Cartilage

Influence of a Silicone Gel (Dermatix®) on Thoracic Scar Formation After Harvesting of Autologous Rib Cartilage for Standardised Total Ear Reconstruction

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
University Hospital Schleswig-Holstein · Academic / Other
Sex
All
Age
9 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGSilicone gel (Dermatix®)The half one the scar to treat was randomised among patients. After regular cleaning of the skin around the scar one half was thinly creamed with the silicone gel from medial to lateral and let dry for 5 minutes. It was done twice daily.

Timeline

Start date
2007-01-01
Completion
2009-01-01
First posted
2007-11-30
Last updated
2007-11-30

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00565552. Inclusion in this directory is not an endorsement.