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Tailored feeding plans could give preemies a healthier start

NCT ID NCT07364500

Prevention Sponsor: Institute of Health Information and Statistics of the Czech Republic Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a personalized nutrition plan for premature infants born before 32 weeks. The plan uses a special software to adjust nutrients based on weekly milk analysis and growth checks. The goal is to prevent health complications and support better growth. 400 infants across Czech hospitals will take part.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Personalized nutrition plan using advanced clinical nutrition software
What this could lead to
If successful, this could establish a national standard for feeding preterm infants, reducing health risks and improving long-term development.
What could go wrong
This is an early pilot study, so results may not be conclusive. The approach may not work for all infants or in all hospitals.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 400 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2025

Expected to finish

Feb 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

22 to 32 weeks

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Preterm infants

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    5 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Brno University Hospital

    NOT_YET_RECRUITING

    Brno, Czech Republic, Czechia

  • General University Hospital

    RECRUITING

    Prague, Czech Republic, Czechia

  • Tomáš Baťa Regional Hospital in Zlín

    RECRUITING

    Zlín, Czechia

  • University Hospital Olomouc

    RECRUITING

    Olomouc, Czech Republic, Czechia

  • České Budějovice Hospital

    RECRUITING

    České Budějovice, Czech Republic, Czechia

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