Analyzing lipid profiles in plasma microparticles from healthy donors

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on the characterization of extracellular vesicles, specifically microparticles, in the plasma of healthy donors. By collecting blood samples, the study aims to analyze the lipid content of these microparticles, which are known to play a significant role in intercellular communication and various biological processes. The findings could provide insights into the potential use of microparticles as biomarkers for early disease management and therapeutic targets. The study involves healthy volunteers who meet specific eligibility criteria for participation.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Person who has given his/her non-opposition
* All healthy volunteers are eligible to donate according to EFS criteria.

Exclusion Criteria:

* Person subject to a legal protection measure (curatorship, guardianship, etc)
* Pregnant, parturient or breast-feeding women
* Adults who are incapable or unable to give their consent
* Minors
* Person not eligible to donate according to EFS criteria.

Where it's running

• Chu Dijon Bourgogne
  Dijon, France Recruiting

Study contacts

• Study coordinator: Damien LELEU
• Email: Damien.leleu@chu-dijon.fr
• Phone: 0380669248

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.