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Can a simple feeding change help sick kids get better nutrition?

NCT ID NCT05286177

What the study statuses mean

This study's is highlighted.

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at whether adjusting tube feeding based on total daily volume, rather than a fixed hourly rate, helps critically ill children get more of the nutrition they need. The trial involves 20 children in the pediatric ICU and aims to see if this approach is practical for a larger future study. It does not test whether the method improves health outcomes directly.

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 lead to a larger study that may improve how tube-fed children in intensive care receive nutrition, potentially helping them recover faster.
What could go wrong
This is a very small feasibility trial with only 20 children, so it cannot prove any health benefits. The main goal is to see if the study methods work, not to test effectiveness.

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 20 people

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

Started

Mar 2024

Expected to finish

Apr 2027

An estimate. End dates often move.

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

1 month to 18 years

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: * Children 1-month post-natal age to 18 years of age * Children anticipated by the intensivist or nurse practitioner to be admitted to the PICU for ≥ 48 hours * Children who will be initiated on EN support Exclusion Criteria: * Children will not be eligible for this study if they are palliative * Children who have contraindications to EN (i.e., a non-functional GI tract) * Children who are on parenteral nutrition * Children who are being fed by a bolus feed regime * Children who cannot progress past trophic feed volumes within 24 hours of EN initiation * Children anticipated to be admitted to PICU for \<48 hours

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Alberta Children's Hospital

    Calgary, Alberta, 73b6a8, Canada

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