Actively Recruiting
Assessment of Neurofilaments Levels in Premature Newborns: Study of Their Early Development
Led by Centre Hospitalier Universitaire de Liege · Updated on 2025-12-12
15
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Universitaire de Liege
Lead Sponsor
C
Centre Hospitalier Régional de la Citadelle
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a prospective observational study aiming to establish reference values of neurofilaments in late preterm newborns (34-37 weeks of gestation) and to evaluate their early postnatal evolution. Neurofilaments are neuronal proteins released into the blood when nerve cells are damaged. They have emerged as promising biomarkers in neurodegenerative diseases, particularly in spinal muscular atrophy (SMA), where higher levels are associated with disease activity. However, very limited data exist on the normal dynamics of neurofilament levels in preterm infants. In this study, up to 15 preterm newborns hospitalized in the neonatal unit will be enrolled (5 at 34 weeks, 5 at 35 weeks, 5 at 36 weeks of gestation). A maximum of 1 mL of additional blood will be collected only during routine clinically indicated blood draws, at birth, on day 2, and weekly until 37 weeks of gestation. Samples will be analyzed for neurofilament concentrations and compared across gestational ages, over time, and with existing data from term newborns and SMA patients. The expected outcome is to generate normative data on neurofilament levels in late preterm infants, which will help interpret biomarker values in future studies and optimize early diagnosis and treatment strategies for neurodegenerative diseases such as SMA.
CONDITIONS
Official Title
Assessment of Neurofilaments Levels in Premature Newborns: Study of Their Early Development
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Gestational age between 34 and 37 weeks of amenorrhea
- Blood test scheduled for clinical reasons
- Signed parental consent
You will not qualify if you...
- Known neurological disorders
- Severe congenital malformations
- Medical contraindication to blood sampling
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hopital Citadelle
Liège, Belgium, 4000
Actively Recruiting
Research Team
T
Tamara Dangouloff, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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