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Clinical Trial Summary

The goal of this observational study is to compare a novel dermal substitute to a the current standard procedure in the treatment of full thickness skin defects. The main questions aim to answer are: • Is the skin elasticity treated with the novel dermal substitute better than the skin elasticity treated with the current standard procedure Participants skin elasticity will be measured by Cutometer® MPA-580 assessment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06255990
Study type Observational
Source University Children's Hospital, Zurich
Contact Sophie Böttcher, MD
Phone +41442667111
Email sophie.boettcher@kispi.uzh.ch
Status Recruiting
Phase
Start date January 15, 2024
Completion date June 2027

See also
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