Actively Recruiting
Prospective Collection of Clinical Data and Human Body Material (HBM) of Cutaneous Melanoma and Non Melanoma Patients. Biobank Huidkanker
Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2025-12-12
7500
Participants Needed
1
Research Sites
1310 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to set up a prospective, fit-for-purpose collection of human body material (HBM)-blood (serum, plasma, DNA) and tissue-and standardized clinical data of patients with cutaneous melanoma and non-melanoma skin cancer. The main questions it aims to answer are: * To create a biobank with samples of human body material (HBM): blood (serum/plasma/DNA) and tissue and clinical data of patients with cutaneous melanoma and non-melanoma. * To support future research questions (after specific approval of the Ethics Committee) by using the biobank (through satellite protocols). If there is a comparison group: Not applicable (umbrella protocol for collection only). Participants will: * Share demographics, medical and surgical history, risk factors. * Complete Cancer Worry Scale questionnaire. * Provide biological samples: * Blood samples (serum, plasma, DNA). * Tissue samples (residual tissue or additional biopsy if consented).
CONDITIONS
Official Title
Prospective Collection of Clinical Data and Human Body Material (HBM) of Cutaneous Melanoma and Non Melanoma Patients. Biobank Huidkanker
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures
- Adult subjects (>18 years of age) at time of enrolment
- Subjects diagnosed with cutaneous melanoma or Non-melanoma skin cancer
- Adult subjects able and willing to provide informed consent
You will not qualify if you...
- Subjects unable or not willing to provide informed consent
- Pregnancy (or willing to become pregnant) is NOT an exclusion criteria (unless specified in the respective satellite protocols)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UZLeuven, Department of Dermatology
Leuven, Vlaams-Brabant, Belgium, 3000
Actively Recruiting
Research Team
A
Annemiek Leeman, Prof. Dr.
CONTACT
S
Sofie Van Kelst, BSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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