About this trial
This is a pilot, single-center, feasibility study to evaluate a new 3D printing method for ORDP design.
To our knowledge, there is no technical or clinical evaluation of ORDPs, particularly in the treatment of hypertrophic scars. The aim of our study is therefore to assess the feasibility of an innovative method of designing ORDPs for the curative treatment of post-burn hypertrophic scars, using a 3D printing process, and to describe the procedures (production time and cost).
Eligibility criteria
Qualifiers
Adult Patients aged > 18 years old
Patient with at least one hypertrophic burn scar in the process of healing localized on a skin area that can benefit from a compression garment and requiring the use of an ORDP
Patient able to give informed consent
Patient affiliated to a social security scheme
Disqualifiers
Patients under guardianship, curatorship or safeguard of justice
Pregnant or breast-feeding women
Trial design
Treatments tested in this trial
- 3D scan measurment