Protocol-driven Nutrition in Preterm Infants
NCT07364500 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 400
Last updated 2026-01-23
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.
Conditions
- Preterm Infants
Interventions
- DIETARY_SUPPLEMENT
-
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.
Sponsors & Collaborators
-
General University Hospital, Prague
collaborator OTHER -
University Hospital Olomouc
collaborator OTHER -
České Budějovice Hospital
collaborator OTHER -
Tomáš Baťa Regional Hospital in Zlín
collaborator UNKNOWN -
Brno University Hospital
collaborator OTHER -
Institute of Health Information and Statistics of the Czech Republic
lead OTHER_GOV
Principal Investigators
-
Richard Plavka, prof. · General Hospital University in Prague
-
Jiří Dušek, M.D., MHA · České Budějovice Hospital
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Weeks
- Max Age
- 32 Weeks
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-08-21
- Primary Completion
- 2026-11-30
- Completion
- 2027-02-28
Countries
- Czechia
Study Locations
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