Ireland
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Recruiting Observational

French Clinical Datbase of Melanoma Patients (RIC-Mel)

NCT03315468 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2012-03-01
Last updated
2025-07-22

Condition(s) studied

Melanoma (Skin)

Study summary

With a high incidence, low survival rates and limiter availability of effective treatment, melanoma is one of the research priorities for health authorities. Optimizing the development of both academic and private research requires the availability information on the features of patients.

To meet this need, the French Multidisciplinary Melanoma Group (GMFMel) in collaboration with INCa (French National Cancer Institute), the CeNGEPS (National Centre for Healthcare Products Trial Management) and the CIC-BT0503 from Nantes University Hospital (Biotherapy Clinical Centre of Investigation) has set up in April 2011 a Clinical Investigation Network for melanoma, called the CeNGEPS-GMFMel network. Nowadays, the network is named :

RIC-Mel : network for Research and Clinical Investigation on Melanoma. Aims of the network are to promote translational and epidemiological projects as well as to optimize the achievements of clinical trials.

To achieve these goals, a database was launched in 2012 that gives a permanently updates mapping of melanoma treated in France with the key information needed for any research projects.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient with melanoma, of any stage, * Patient agreed to participate. Exclusion Criteria: * Individuals under court protection

Primary outcome measure(s)

  • Overall survival of melanoma patients included in the RIC-Mel database — 5 years
    Overall survival if defined as the time between the primary melanoma tumour removal and the death or the date of data extraction from the RIC-Mel database for alive patients.

Trial sites (1)

FacilityCityRegionStatus
Nantes University Hospital Nantes France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03315468 on ClinicalTrials.gov ↗ ← All trials in France