Actively Recruiting

Age: 0Days - 14Days
All Genders
NCT07402083

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

Age: 0Days - 14Days
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Hospital Universitario y Politécnico La Fe

Valencia, Valencia, Spain, 46026

Actively Recruiting

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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

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