Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2025-05-01
2027-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Study Groups
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1
Retrospective
No interventions assigned to this group
2
Prospective
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Minimum age 18 years
* Consent to participate in the study (signing of patient consent) should be presented in vTB+ according to the doctor, based on the disease/diagnosis, especially in the case of:
* Malignant melanoma from stage IIB
* Malignant melanoma and stage shift/recurrence o Extracutaneous melanoma o Cutaneous lymphoma from stage Ib o Problem cases with malignant, epithelial tumors (BCC, SCC) with interdisciplinary issues, e.g. complicated localization, extension/ infiltration (e.g. Ulcus rodens, Ulcus terebrans), metastasized tumors, immunosuppressed patients o all rare malignant skin tumors (including Merkel cell carcinoma, DFSP, MFH, leiomyosarcoma, S., Kaposi's sarcoma, angiosarcoma), regardless of stage o severe side effects from drug-based tumor therapy • is an external patient: An external patient is someone who receives tumor therapy exclusively or in co-treatment in the branch or in an external clinic (in distinction to patients without prior treatment for initial presentation at the CCC) . This also applies to patients who are only seen once at the vTB.
In this case, revenue/cost aspects and the DKG requirement are ignored. This means that so-called external patients can also be treated at the center, including initiation of therapy. The decisive factor is the presentation of the external patient (personal presentation of the external patients is not mandatory) and that external co-treaters are consistently informed and involved.
* has a medical license
* has dermatological patients who are eligible to be presented in the vTB+
Exclusion Criteria
* Linguistic or other limitations (such as dementia) that prevent independent consent to the privacy policy.
* No consent to participate in the study (patient consent) or withdrawal of consent during the course of the study In addition, external physicians will be excluded from the study if no joint cooperation agreement can be negotiated and signed.
18 Years
ALL
No
Sponsors
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Deutsche Krebshilfe e.V., Bonn (Germany)
OTHER
University Hospital, Bonn
OTHER
University Hospital Dresden
OTHER
University Hospital Muenster
OTHER
Responsible Party
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Principal Investigators
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Philipp Lenz, MD
Role: PRINCIPAL_INVESTIGATOR
Westdeutsches Tumorzentrum Münster, Universitätsklinikum Münster
Locations
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Abteilung für Integrierte Onkologie - CIO Bonn, Universitätsklinikum Bonn
Bonn, , Germany
Nationales Centrum für Tumorerkrankungen Klinik u. Poliklinik für Dermatologie, Universitätsklinikum Dresden
Dresden, , Germany
Westdeutsches Tumorzentrum Münster, Universitätsklinikum Münster
Münster, , Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2025-275-b-S
Identifier Type: OTHER
Identifier Source: secondary_id
BO ff (Multi)-EK-16012025
Identifier Type: -
Identifier Source: org_study_id
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