Probiotics show promise for constipation in kids with cerebral palsy
NCT ID NCT07393256
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether daily probiotic supplements could improve constipation and weight gain in 30 children with cerebral palsy. Participants took either Lactobacillus reuteri or a prebiotic-enriched Lactobacillus rhamnosus for 28 days. Caregivers tracked bowel movements and stool consistency using a diary. The goal was to see if these supplements are safe and effective for easing constipation and supporting better nutrition.
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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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Nov 2022
- Finished
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Apr 2025
- Lead sponsor
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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
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6 months to 18 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: * Age between 6 months and 18 years * Clinical diagnosis of cerebral palsy * Gross Motor Function Classification System (GMFCS) levels III, IV, or V * Chronic constipation diagnosed according to Rome IV criteria * Stable medical condition * Ability to receive oral or enteral nutrition Exclusion Criteria: * Cerebral palsy due to degenerative neurological disorders * Constipation due to a known organic cause * Congenital gastrointestinal tract malformations * Inflammatory bowel disease * Metabolic diseases * History of kidney failure * Use of antibiotics, probiotics, or prebiotics within one month prior to enrollment * Anticipated poor adherence to the study protocol * Requirement for hospitalization during the study period
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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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Ordu University Faculty of Medicine, Department Of Pediatric Surgery
Ordu, Outside of the US, 52200, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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