Prospective Collection of Clinical Data and Human Body Material (HBM) of Cutaneous Melanoma, Non Melanoma Patients and Healthy Controls. Biobank Huidkanker

Recruiting now

Conditions studied: Skin Cancer, Non-Melanoma, Skin Cancer Melanoma

In brief

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, non-melanoma skin cancer and healthy controls. 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, non-melanoma and helathy controls. * 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).

Key facts

Study ID

NCT07266142

Run by

Universitaire Ziekenhuizen KU Leuven

People needed

7500

Starts

2025-11-17

Expected to finish

2051-01-01

Last updated by the study team

2026-06-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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, Non-melanoma skin cancer or healthy controls.
• Adult subjects able and willing to provide informed consent.

You may not qualify if…

• 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.

Where it is running

• UZLeuven, Department of Dermatology — Leuven, Vlaams-Brabant, Belgium (enrolling)

Full record on ClinicalTrials.gov

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