About this trial
The aim of this study is to use MRI and Vectra metadata from patients in order to develop the "customizable" aspect of the MyBREAST One implant through computer modeling of this implant based on the collected metadata.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The targeted patients will be those undergoing mastectomy following neoadjuvant chemotherapy, prophylactically, or in the context of lobular cancer.
Disqualifiers
None
Trial population
Patients from the Plastic and Maxillofacial Surgery Department of CHU Liège.
Trial design
Case-only
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Extraction from medical records of a copy of MRI and Vectra XT 3D images
For patient undergoing mastectomy after neoadjuvant chemotherapy, consent to use MRI and Vectra images will be requested during chemotherapy when the Vectra is taken. MRI will be extracted from medical records.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: