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New Real-Food tube feed put to the test in kids

NCT ID NCT07036081

What the study statuses mean

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study looked at whether children aged 3 to 15 who need feeding through a tube would accept and tolerate a new formula made from real food called Wilbo's Blends+. For one week, participants used the formula as part of their regular feeding plan, and parents recorded any stomach issues like bloating or vomiting. The goal was to see if this real-food option is easy to use and comfortable for children.

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

45 people

The number who actually took part.

Started

Oct 2025

Finished

Mar 2026

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 to 15 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 and young people (age 3-15) who are assessed by a Doctor or Dietitian as requiring enteral tube feeding via gastrostomy. * Children and young people able to receive a minimum of 30% of their daily intake from the study product for at least 7 consecutive days. * Participant is capable of communication/filling in the questionnaires or having a parent/carer who can answer the questions by close observation of the participant reactions. If there are any communication issues the research dietitian/nurse should support. Written, informed consent from the parent/carer/guardian and assent from the participant obtained. Exclusion Criteria: * \<3 years old * \>15 years old * Total Parenteral Nutrition * Post pyloric enteral feeding * Enteral tube feeding via Nasogastric tube * Patients with severe renal, oncology, metabolic, IBD or hepatic conditions who are considered clinically unstable * Known food allergies or intolerances to any ingredient in the product * Requirement of a fibre free feed (e.g. IBD) * Children who had an inability to comply with the study protocol, in the opinion of the investigator * Children who have been involved in another interventional study within 2 weeks of this study. * Children with recent changes (within 1 week) in medication used to manage gastrointestinal symptoms

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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

  • Nottingham University Hospitals NHS Trust

    Nottingham, Nottinghamshire, NG7 SUH, United Kingdom

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