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Porridge study: which corn meal keeps you full longer?

NCT ID NCT07204470

Knowledge-focused Sponsor: PepsiCo Global R&D 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how four different instant maize porridges affect hunger and fullness. Fifty healthy adults aged 18-35 with normal weight took part. They ate the porridges after fasting overnight and reported their appetite, plus gave blood samples to measure hunger-related hormones and blood sugar. The goal was to see if whole-grain maize porridge keeps people fuller longer than other types.

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

50 people

The number who actually took part.

Started

Jul 2025

Finished

Aug 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Ages

18 to 35 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Availability to participate on the test days * Interest and consent to participate in the study * Participants must be willing to fast 10 hours overnight before the test breakfast meal (only water allowed) * Products and meals high in fiber, alcohol and strenuous exercise should be avoided 24 hours before the test * Age 18-35 years * Healthy BMI: 18.5-24.9 kg/m2 * Equal split, males and females Exclusion Criteria: * Pregnancy; breast-feeding * History of gastrointestinal disease having an impact on food absorption or digestion; anorexia nervosa or bulimia nervosa * Anaemia * Hypoglycaemia * Cardiovascular disease; elevated plasma glucose; unstable thyroid function * Abnormal/irregular menstrual cycle * Substance abuse * Being on medication which influences appetite * Depression; smoking * Participation in any weight altering program; weight gain or loss \> 5 kg in 3 months prior to enrolment * History of intestinal discomfort when consuming relatively small (e.g., \<10g) amounts of non-digestible fibres * Any known food allergies or intolerances such as wheat or soy; special diets prescribed by medical practitioner * Any intensive physical training program

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As listed by the trial registrant

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

Satiety

Contacts and locations

Locations

  • U. Pretoria

    Pretoria, 0083, South Africa

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