C43.9
Conditions
Interventions
Group 1: Patients with pigment lesions that are supsicious for malignant melanoma will be included. Our goal is to characterize the molecular changes that occur when cells transition from a benign ne
Sponsors
Charité-Universitätsmedizin Berlin, Klinik für Dermatologie, Venerologie und Allergologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - suspected (premalignant) nevus associated Melanoma - dated and signed informed consent form
Exclusion criteria
Exclusion criteria: - patient wish - immunocompromised patients - participation in another study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Characterization of molecular changes of tumor cells at the transition between benign melanocytic nevi and malignant melanoma. | — |
Secondary
| Measure | Time frame |
|---|---|
| Characterization of molecular changes of cells of the tumor microenviromnet at the transition between benign melanocytic nevi and malignant melanoma. | — |
Countries
Germany
Contacts
Public ContactRose K.C. Moritz
Charité- Universitätsmedizin Berlin, Klinik für Dermatologie, Venerologie und Allergologie
Outcome results
None listed