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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02884362
Other study ID # 16HLCUTA01
Secondary ID
Status Recruiting
Phase N/A
First received July 28, 2016
Last updated August 25, 2016
Start date January 2016
Est. completion date June 2026

Study information

Verified date July 2016
Source Institut Claudius Regaud
Contact Nicolas MEYER, MD PHD
Phone 5 31 15 51 61
Email Meyer.Nicolas@iuct-oncopole.fr
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés
Study type Observational

Clinical Trial 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.


Description:

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


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date June 2026
Est. primary completion date January 2026
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
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 Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
clinical biological data collection on melanoma
collection and centralization of clinical and biological data of patients with melanoma

Locations

Country Name City State
France Institut claudius regaud IUCT ONCOPOLE Toulouse

Sponsors (1)

Lead Sponsor Collaborator
Institut Claudius Regaud

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Database of patients with melanoma 10 years No
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