Analyzing lipid profiles in plasma microparticles from healthy donors
Lipid Characterisation of Plasma Microparticles in a Large Population of Healthy Donors
Centre Hospitalier Universitaire Dijon · NCT06183632
This study looks at tiny particles in the blood of healthy people to see what fats they contain and if they could help in spotting diseases early.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire Dijon (other) |
| Locations | 1 site (Dijon) |
| Trial ID | NCT06183632 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy adults who meet the eligibility criteria for blood donation.
Not a fit: Patients who are pregnant, under legal protection, or unable to provide consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to the identification of new biomarkers for early disease diagnosis and management.
How similar studies have performed: While the specific approach of analyzing microparticles in healthy donors may be novel, similar studies have shown promise in using extracellular vesicles as biomarkers in various conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Dijon
- Chu Dijon Bourgogne — Dijon, France (RECRUITING)
Study contacts
- Study coordinator: Damien LELEU
- Email: Damien.leleu@chu-dijon.fr
- Phone: 0380669248
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Healthy Donor