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Parents' syringe feeding may boost NICU presence for preemies

NCT ID NCT05272956

Knowledge-focused Sponsor: University Hospital, Limoges Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether allowing parents to push a syringe for their premature baby's tube feeding (instead of using a machine) helps them spend more time in the neonatal intensive care unit. 72 babies born between 30 and 34 weeks were included. The main goal was to compare the average hours parents were present between the two feeding methods.

What this could mean

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

What this could lead to
If successful, this could show that involving parents in feeding helps them spend more time with their premature baby in the NICU.
What could go wrong
This is a small, completed study with only 72 babies, so results may not apply to all NICUs. It does not test a new drug or treatment.

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

72 people

The number who actually took part.

Started

Aug 2022

Finished

Nov 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

3 days and older

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: * Gestational age between 30 and 34 WA (weeks of amenorrhea) * Patient affiliated to a social security scheme * Hospitalized in neonatal intensive care unit (NICU) * 3 days of life or more Exclusion Criteria: Corrected age\> 34WA and 4 days * Mechanical ventilation or non-invasive ventilation with FIO2\> 35% * Serious congenital malformation * Planned transfer to another hospital * Enteral nutrition \<40ml / kg / day * Immediate post-operative care * Multiple pregnancy * Poor understanding of french • Secondary exclusion criteria * Digestive rest greater than 5 days * Death * No enteral nutrition pushed by parents

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Conditions

The condition(s) this trial relates to.

Premature Birth

As listed by the trial registrant

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

Premature birth

Contacts and locations

Locations

  • Centre Hospitalier Henri Duffaut

    Avignon, 84000, France

  • Limoges university hospital

    Limoges, 87042, France

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