PLasmatic Extracellular Vesicles AS Biomarkers of nEural Tissue Damage
- Sponsor
- Roberto Furlan
- Study ID
- NCT07769294
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Study Details
Recently proposed central nervous system damage biomarkers detectable in biofluids, such as neurofilament light chain (NfL) have several limits, including a lack in specificity and a kinetic that does not allow them to be used as outcome measures in clinical trials for neurodegenerative diseases such as the progressive forms of multiple sclerosis (MS) or the sequelae of stroke. Our team has pioneered the detection of central nervous system (CNS) extracellular vesicles (EVs) as biomarkers in MS and Alzheimer's Disease. If EVs are not the best solution themselves, we propose also to investigate their content to reveal potential new biomarkers having the same significance and an easier detection technology. Thus, we propose here to set-up front line technologies to detect EVs of CNS origin, or their content, in the plasma of persons affected by MS or by stroke to find better ways to monitor ongoing neurodegenerative processes and therefore allow easier development of new treatments.
Key Dates
- First listed
- Aug 17, 2026
- Start date
- Sep 15, 2026
- Status verified
- Aug 2026
- Primary completion
- Mar 31, 2028
- Completion
- Jul 31, 2028
Study Design
- Enrollment
- 60 participants (estimated)
Arms
- Arm: Multiple SclerosisPersons with multiple sclerosis undergoing diagnostic workup
- Arm: StrokePersons admitted to the Stroke Unit for ischemic stroke
- Arm: Healthy DonorsHealthy donors matched for age and sex
Primary Outcome Measure
Neural plasma extracellular vesicles [ Time Frame: Baseline, 3months, 6months, 12 months for multiple sclerosis. Baseline, and 1, 7 and 14 days after stroke for stroke patients. Once for healthy donors. ]
Central Contacts
- Roberto Furlan, MD, PhD+39 0226434867
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