Actively Recruiting
Administration of Extracellular Vesicles From Donor Human Milk in Preterm Infants
Led by Instituto de Investigacion Sanitaria La Fe · Updated on 2026-02-11
20
Participants Needed
1
Research Sites
203 weeks
Total Duration
On this page
Sponsors
I
Instituto de Investigacion Sanitaria La Fe
Lead Sponsor
H
Hospital Universitario La Fe
Collaborating Sponsor
AI-Summary
What this Trial Is About
The AdVEMPrem study is exploring whether tiny particles called extracellular vesicles (EVs), which are naturally found in human milk, can help protect very premature babies from serious gut problems such as necrotizing enterocolitis (NEC). NEC is a dangerous condition that affects the intestines of preterm infants and can lead to long-term health issues. Human milk is the best nutrition for babies, but when a mother's own milk is not available, donor human milk (DHM) is used. EVs in milk carry proteins, fats, and genetic material that may support gut development, immunity, and brain growth. While laboratory studies suggest EVs are beneficial, their effects in premature babies have not yet been proven. In this study, 20 very preterm infants (\<32 weeks of gestation) will be enrolled during their stay in the Neonatal Intensive Care Unit (NICU). All babies in the study will receive oral supplementation with EVs isolated from donor human milk. Researchers will monitor feeding tolerance, growth, intestinal health, and early development. Blood and urine samples will also be collected to study how EVs affect metabolism and stress markers. The main goal is to see if EV supplementation is safe and well tolerated. Longer-term follow-up will explore whether EVs improve growth and neurodevelopment as the babies grow. This research could lead to new nutritional strategies to reduce NEC and improve outcomes for premature infants and their families.
CONDITIONS
Official Title
Administration of Extracellular Vesicles From Donor Human Milk in Preterm Infants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Preterm infants born at <32 weeks gestational age
- Age between 0 and 14 days of life at enrollment
- At risk of developing necrotizing enterocolitis (NEC)
- Written informed consent obtained from parent(s) or legal guardian(s)
You will not qualify if you...
- Major congenital anomalies or chromosomal abnormalities
- Severe gastrointestinal malformations (e.g., gastroschisis, intestinal atresia)
- Conditions incompatible with enteral feeding or EV supplementation
- Participation in another interventional clinical trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital Universitario y Politécnico La Fe
Valencia, Valencia, Spain, 46026
Actively Recruiting
Research Team
J
Julia Kuligowski, PhD
CONTACT
M
María Gormaz, PhD, MD
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
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here