Database for melanoma patients in France
Official title: French National Cohort of Patients With Melanoma (Any Stage). Network for Research and Clinical Investigation, the RIC-Mel Network.
Run by Nantes University Hospital · NCT03315468 · Data updated 2026-11-12
This study is creating a database of melanoma patients in France to help researchers and doctors better understand the disease and improve treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 16000 (estimated) |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 1 site (Nantes) |
| Status | Recruiting |
| Started | March 1, 2012 |
| Main results expected | March 1, 2030 |
| Study ends | March 1, 2030 |
| Registry record updated | July 22, 2025 |
| Trial ID | NCT03315468 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with melanoma at any stage who agree to participate.
✕Probably not a fit
Patients with melanoma who do not consent to participate will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The RIC-Mel network is a collaborative initiative aimed at improving melanoma research by creating a comprehensive database of patients diagnosed with melanoma across France. This observational study collects key clinical data from various participating centers, including public and private dermatology and cancer centers. The database facilitates access to vital information for researchers and clinicians, promoting translational and epidemiological projects while optimizing clinical trial outcomes. The initiative is supported by prominent institutions and has received ethical approval for data confidentiality.
Why it matters
Potential benefit: If successful, this database could enhance the understanding of melanoma and improve treatment strategies for patients.
How similar studies have gone: Other studies utilizing similar database approaches have shown success in enhancing melanoma research and treatment outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient with melanoma, of any stage, * Patient agreed to participate. Exclusion Criteria: * Individuals under court protection
Where it's running
-
Nantes University Hospital
Nantes, France Recruiting
Study contacts
- Principal investigator: Gaëlle Quereux, PU-PH — Nantes University Hospital
- Study coordinator: Gaëlle Quereux, PU-PH
- Email: gaelle.quereux@chu-nantes.fr
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Assessing the safety and effectiveness of ENV-501 in patients with HER3-expressing solid tumors
This study is testing a new treatment called ENV-501 to see if it is safe and effective for people with advanced solid tumors that express HER3, like melanoma, lung cancer, and breast cancer.
-
Assessing a test to predict treatment response in advanced melanoma patients
This study tests if the IOpener® melanoma test can help predict how well treatment will work for people with advanced melanoma who are starting their first-line therapy.
-
Monitoring the effects of encorafenib and binimetinib in melanoma treatment
This study is testing how the levels of two melanoma drugs, encorafenib and binimetinib, affect side effects and treatment success in adults with a specific type of advanced melanoma.
-
Using Cyclophosphamide and Pembrolizumab for advanced melanoma treatment
This study is testing if a combination of Cyclophosphamide and Pembrolizumab can help people with advanced melanoma who haven't responded to other treatments feel better and improve their health.
-
Skipping full lymph node removal for stage III melanoma patients who show a strong response in the index node
This trial will see if patients with resectable stage III melanoma who get neoadjuvant ipilimumab plus nivolumab and show a major pathological response in the index lymph node can safely avoid therapeutic lymph node dissection.
-
Evaluating the DermaSensor device for detecting melanoma
This study is testing a new device to see if it can accurately detect skin lesions that might be melanoma in people aged 40 and older.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.