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RecruitingNCT02884362Updated Aug 31, 2016

Prospective Melanoma Database

An observational study in Melanoma, sponsored by Institut Claudius Regaud. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-08-31.

Sponsored by Institut Claudius Regaud · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2026, 9 months ago, but the record still lists the study as recruiting.
Study type
Observational
Time perspective
Prospective
Enrollment
10,000
Ages
18 Years and older
Sex
All
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Study summary

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.

Read the detailed description

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

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Conditions studied

  • Melanoma

Browse trials for

Keywords

  • melanoma clinical biological database
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In context

Melanoma

3,006 studies on the registry are indexed under Melanoma; 520 are open to participants now.

This study's planned enrollment of 10,000 is above the median of 182 across 438 observational studies indexed under Melanoma.

Browse Melanoma studies →

Lead sponsor

Institut Claudius Regaud is the lead sponsor of 117 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with any histological type of melanoma and of any stage

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

Exclusion Criteria:

  • Any psychiatric or medical condition that would make the patient unable to give a signed informed consent
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Study design

Time perspective
Prospective
Enrollment
10,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Interventions

  • Otherclinical biological data collection on melanoma

    collection and centralization of clinical and biological data of patients with melanoma

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What researchers measure

Primary outcomes

  1. Database of patients with melanoma

    Time frame: 10 years

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Study locations

1 of 1 sites recruiting
  • Institut claudius regaud IUCT ONCOPOLE
    Toulouse, 31059, France
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02884362
Lead sponsor
Institut Claudius Regaud
Responsible party
Sponsor
First posted
Aug 31, 2016
Start date
Jan 2016
Primary completion
Jan 2026 (estimated)
Completion
Jun 2026 (estimated)
Last update
Aug 31, 2016

Study contacts

Nicolas MEYER, MD PHD
Contact
Meyer.Nicolas@iuct-oncopole.fr
5 31 15 51 61 ext. 33
Nicolas MEYER, MD PHD
principal investigator · Institut claudius regaud Toulouse ONCOPOLE

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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