Actively Recruiting
Measuring the Metabolome in Melanoma Patients Using NMR Spectroscopy and Gas Chromatography to Explore Disease Differences
Led by Technische Universität Dresden · Updated on 2025-01-09
3000
Participants Needed
1
Research Sites
256 weeks
Total Duration
On this page
Sponsors
T
Technische Universität Dresden
Lead Sponsor
U
University Hospital Carl Gustav Carus
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating how the metabolome—the collection of small molecules in blood, body fluids, and tissues—differs between patients with malignant melanoma at various tumor stages and healthy individuals. The goal is to determine whether these metabolite patterns can help with early detection of melanoma diagnosis, recurrence, or changes in disease stage. This prospective, single-center study focuses on analyzing these differences over time to improve understanding of melanoma progression. Blood and other biosamples are collected and stored in the BioBank Dresden. These samples undergo analyses using Nuclear Magnetic Resonance (NMR) spectroscopy and Liquid Chromatography-Mass Spectrometry (LC-MS). The study plans to use these samples for further metabolomic analyses to explore disease-related changes. Participants are followed on average for about three years during which researchers measure differences in metabolite concentrations. The study tracks changes throughout this period to assess the metabolome's potential as an early marker for melanoma progression or recurrence. This long-term observation allows careful monitoring of metabolite patterns in relation to the disease course.
CONDITIONS
Official Title
The Study Aims to Measure the Metabolome in Melanoma Patients Using NMR Spectroscopy and Gas Chromatography and to Analyse Differences Depending on the Course of the Disease.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current or past history of melanoma
- Ongoing therapy or tumour aftercare at the Skin Cancer Centre at Dresden University Hospital
You will not qualify if you...
- Refusal to participate in the study
- Lack of capacity to consent
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Trial Site Locations
Total: 1 location
1
University Hospital Carl Gustav Carus
Dresden, Saxony, Germany, 01307
Actively Recruiting
Research Team
F
Frank Friedrich Gellrich, Dr. med.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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