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Prospective Melanoma Database

Recruiting
18 years of age
Both
Phase N/A

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Overview

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.

Description

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

Eligibility

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

Study details

Melanoma

NCT02884362

Institut Claudius Regaud

25 January 2024

Step 1 Get in touch with the nearest 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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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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