Prospective Melanoma Database

  • End date
    Jun 21, 2026
  • participants needed
  • sponsor
    Institut Claudius Regaud
Updated on 23 February 2022


In research on melanoma, translational research is the essential link between basic research and clinical research by facilitating the passage between discovery and improvement in the quality of patients care.That is the reason why it is very important to collect, and centralize clinical and biological data of patients with melanoma.

The aim of the project is to provide to scientific community a structured, mixed clinical and biological database, unique in France, in order to insure accessibility to clinical data.


collection of clinical and biological data from patients with melanomas of any stage in a structured and centralized database

Condition Melanoma
Treatment clinical biological data collection on melanoma
Clinical Study IdentifierNCT02884362
SponsorInstitut Claudius Regaud
Last Modified on23 February 2022


Yes No Not Sure

Inclusion Criteria

Age > 18 years
Histologically confirmed melanoma of any stage
Affiliated to a social security system in france
Who signed the informed consent

Exclusion Criteria

Any psychiatric or medical condition that would make the patient unable to give a signed informed consent
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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