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Clinical Trials in Czechia / NCT07364500
Recruiting Not applicable

Protocol-driven Nutrition in Preterm Infants

NCT07364500 · tracked via the Priya Life Science Czechia tracker
Phase
Not applicable
Started
2025-08-21
Last updated
2026-01-23

Condition(s) studied

Preterm Infants

Investigational drug(s) / intervention(s)

Nutrition plan supported by advanced clinical nutrition software

Nutrition plan supported by advanced clinical nutrition software: Infants undergo regular anthropometric assessments (weight, length, head circumference), and detailed fluid and nutrient intake is recorded. Weekly analysis of the macronutrient composition of maternal or donor milk is conducted, enabling personalized fortification to meet the infant's current needs. The intervention utilizes a dedicated nutrition software tool, incorporating Fenton growth charts, to support clinical decisions and track progress via z-scores compared to term-born infants. By aligning nutrient supply with individual requirements and promoting early enteral feeding, the project seeks to enhance growth outcomes, minimize risks such as bronchopulmonary dysplasia or retinopathy, and shorten the length of stay in neonatal intensive care.

Study summary

The project is a national, prospective, multicenter, interventional pilot project focused on protocol-driven nutrition in preterm infants in the Czech republic.

The primary aim of the project is to prepare, test, and develop a proposal for a national methodology for the care of preterm newborns in the field of nutrition. This will reduce health risks in premature infants and minimize the negative impacts on the overall development of the child and the family of the premature infant.

Eligibility

Sex
ALL
Min age
22 Weeks
Max age
32 Weeks
Healthy volunteers
No
Inclusion Criteria: * Infants born before 31+6 weeks gestation. * Signed consent for participation in the project and consent for the processing of personal data. * Admission to neonatal care in the participating hospital within 24 hours after birth. Exclusion Criteria: * Congenital malformations. * Fetal hydrops. * Intraventricular hemorrhage requiring drainage. * Necrotizing enterocolitis requiring surgical treatment. * Surgically treated hydrocephalus. * Unsigned consent for participation in the project and/or consent for the processing of personal data.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Brno University Hospital Brno Czech Republic Not Yet Recruiting
České Budějovice Hospital České Budějovice Czech Republic Recruiting
University Hospital Olomouc Olomouc Czech Republic Recruiting
General University Hospital Prague Czech Republic Recruiting
Tomáš Baťa Regional Hospital in Zlín Zlín Czechia Recruiting

More Institute of Health Information and Statistics of the Czech Republic trials in Czechia

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07364500 on ClinicalTrials.gov ↗ ← All trials in Czechia