N62
Conditions
Interventions
Group 1: A total of 40 female patients who underwent reduction mammaplasty between June 2017 and July 2025 will be included in the study.
To generate the three-dimensional surface models, two imaging
Sponsors
Universitätsklinikum Regensburg
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Female patients who underwent reduction mammaplasty between June 2017 and July 2025, who have provided written informed consent to participate in the study, and who are of legal age.
Exclusion criteria
Exclusion criteria: Refusal to participate; allergy to adhesive markers; severe complications that significantly impede or prevent imaging; pregnancy or breastfeeding at the time of imaging.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of anthropometric measurements and breast surface models obtained with a smartphone-based system and a conventional 3D surface scanner. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of two surgical techniques for reduction mammaplasty (T-scar and U-scar) | — |
Countries
Germany
Contacts
Public ContactVanessa Brébant
Universitätsklinikum Regensburg
Outcome results
None listed