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NCT Number: NCT06747260

Feasibility and Safety of Intranasally Administered Breast Milk in HIE

This is a prospective intervention single center study to evaluate the feasibility and safety of intranasal breast milk in hypoxic-ischaemic encephalopathic neonates receiving therapeutic hypothermia.

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Key information

About this study

Perinatal asphyxia and the resulting hypoxic-ischemic encephalopathy (HIE) are the leading cause of neonatal mortality and long-term neurodevelopmental disabilities. Based on our current knowledge, therapeutic hypothermia is the only therapy that has been proven to reduce central nervous system damage in HIE neonates. Improving neurodevelopmental outcomes of newborns with HIE has been an intense area of research over the past decade.

Breast milk is a complex biological substance that contains a variety of bioactive components including neurotrophic growth factors, cytokines, immunoglobulins, and multipotent stem cells. Studies have shown that exclusive breastfeeding in the early stages of development has a positive impact on cognitive outcomes. Animal studies support that mesenchymal stem cells and neurotrophic substances found in breast milk, when administered intranasally enter the central nervous system and reduce the extent of neurological damage. In preterm infants, it has been shown that intranasally administered breast milk is safe and well-tolerated.

In this prospective study our aim is to assess the feasibility and safety of intranasally delivered breast milk to HIE infants treated with hypothermia. Our objective is to administer fresh, own-mother's breast milk intranasally to neonates with HIE starting from the first day of life and continuing for 1 month.

Feasibility will be based on the ability to initiate treatment within 48 hours of birth using own mother's fresh milk expressed within 4 hours and continuing treatment after discharge until day 28. Safety will be assessed through monitoring vital signs and documenting any adverse events. Time to reach full enteral feeding and lengths of exclusive breast feeding will be recorded and analyzed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Moderate or severe hypoxic- ischaemic encephalopathy, receiving therapeutic hypothermia
  • ≥ 35. gestational week
  • < 48 hours of life
  • Hypothermia treatment for 72 hours
  • Parental consent form

Exclusion criteria

  • Congenital malformation
  • Concurrent cerebral lesions
  • ECMO therapy
  • Contraindication of lactation
  • Mother unable or unwilling to provide fresh breast milk
  • Postpartum asphyxia

Treatment and study plan

Intranasal breast milk

Biological

Neonates with hypoxic-ischemic encephalopathy receive their own-mother's fresh breast milk intranasally, starting from the first 48 hours of life and continuing for 28 days. Dose: 2 times daily, 0.4 ml in each nostril (15 minutes apart).

Primary outcomes

  1. Proportion of patients where treatment was initiated within 48 hours

    Time frame: 1 months

    Feasibility will be based on the ability to initiate treatment within 48 hours of birth using own mother's fresh milk.

Secondary outcomes

  1. Number of adverse events associated with breast milk administration

    Time frame: 1 month

    Number of adverse events associated with breast milk administration will be recorded, including desaturation (SpO2<80%), bradycardia (heart rate <70% of baseline), apneic episode requiring bag and mask ventilation within 5 minutes of the intervention, or an increase in respiratory support (mode, setting, or FiO2 increase >10%) within 1 hour of the intervention.

  2. Time to reach full enteral feeding

    Time frame: 1 month

    Time to reach full enteral feeding will be recorded and analyzed as a secondary outcome.

  3. Length of exclusive breast feeding

    Time frame: 2 years

    Lengths of exclusive breast feeding will be recorded and analyzed as a secondary outcome.

  4. Total number of treatments during first months of life

    Time frame: 1 months

    Total number of treatments administered in hospital and at home during the first months of life

Study contacts

Contact information is provided by the study sponsor or research team.

Agnes Jermendy, MD, PhD

CONTACT

[email protected]

+36204600798

Unoke Meder, MD, PhD

CONTACT

[email protected]

+36303987970

Sponsors and collaborators

Lead sponsor

Semmelweis University

Other

Registry information

Official study title

Feasibility and Safety of Intranasal Breast Milk in Hypoxic-ischaemic Encephalopathy

Acronym: F-NEO-BRIGHT

Important dates

Study start
2024
Primary completion
2025
Study completion
2030
First posted
Dec 24, 2024
Registry last updated
May 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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