New vitamin supplements aim to make life easier for kids with rare metabolic disorders
NCT ID NCT07619170
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests new vitamin and mineral supplements called EasiVits for children aged 1-16 with inborn errors of metabolism (IEM). These supplements have less carbohydrate and no flavor, so they can be used with different diets and kids can add their own taste. The goal is to see if children find them more acceptable and easier to tolerate than current supplements. About 30 children will try EasiVits for 7 days, and researchers will track how well they take them and any stomach issues.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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30 people
The number who actually took part.
- Started
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Mar 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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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
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1 year to 16 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male and female IEM patients ages 1-16 years. * Patients diagnosed with an IEM. * Taking vitamin and mineral supplements for IEM and willing to take the new supplements for 7 days. * Absence of comorbidities. * Adherence with dietary management and vitamin and mineral supplements. * Able to understand and comply with the requirements of the investigation and sign the Informed Consent Form/Assent form. Exclusion Criteria: * Age \<1 years old. * Patients with comorbidities. * Any moderate to severe acute illness which in the opinion of the Investigator would interfere with the study procedures or study outcome. * History of poor co-operation, non-adherence with dietary management, or poor adherence to investigation procedures. * Participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Birmingham Children's Hospital
Birmingham, B4 6NH, United Kingdom
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