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Prebiotic EffecT InfanTs

Double-blind, Randomized Placebo-controlled Trial Investigating the Effect of Prebiotic Inulin-type Fructans on Bowel Habits of Infants

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04791956
Acronym
PETIT
Enrollment
140
Registered
2021-03-10
Start date
2021-03-17
Completion date
2024-06-30
Last updated
2023-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diet, Healthy, Healthy, Infant Development

Keywords

Microbiota, gastrointestinal health

Brief summary

The study aims to confirm the effectiveness of chicory-derived prebiotic inulin-type fructans on stool consistency in infants.

Detailed description

The fermentation of prebiotic inulin-type fructans leads to a modulation of the gut microbiota composition, in particular to a growth stimulation of bifidobacteria, and the production of organic acids like lactate and short-chain fatty acids (SCFA). The introduction of solid foods is frequently associated with harder stools which are more difficult to pass and can cause painful defecations. Subsequently, the changes in bowel habits associated with weaning and the introduction of complementary foods could be minimized by the addition of prebiotics to complementary foods and, thus, the transition from milk-feeding to family food could be facilitated.

Interventions

DIETARY_SUPPLEMENTPrebiotic

Daily intake of Inulin-type fructans from chicory

DIETARY_SUPPLEMENTPlacebo

Daily intake of maltodextrin

Sponsors

Hospital Universitari Sant Joan de Reus
CollaboratorOTHER
Hospital de Tarragona Joan XXIII
CollaboratorUNKNOWN
Institut Investigacio Sanitaria Pere Virgili
CollaboratorOTHER
Beneo-Institute
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Months to 12 Months
Healthy volunteers
Yes

Inclusion criteria

* Child is healthy at the time of pre-examination * Child was born on term or preterm (≥ 32 weeks of gestation) * Child is aged 6-12 months at the time of pre-examination (for preterm born children (32-37 weeks of gestation), corrected age will be applied) * Normal growth (weight and length for age between 10th and 90th percentiles, Fenton and Kim 2013) * Child receives at least one meal per day as complementary feeding * Child and legal guardian are able and willing to follow the study instructions * Child is suitable for participation in the study according to the investigator/physician/study personnel * Written informed consent is given by parent or legal guardian

Exclusion criteria

* No legal guardian's command of any local language * Organic causes of defecation disorders incl. Hirschsprung disease, Spina bifida, hypothyroidism etc. * Other metabolic or renal abnormalities or psychomotor retardation (e.g. hypotonia) * Child has allergy to cow's milk protein or lactose intolerance * Child has been or is currently breast-fed more than once daily (6 weeks before intervention) * Child has mostly loose or watery stools in ≥ 50% of defecations * Use of drugs (e.g. antibiotics) influencing gastrointestinal function (6 weeks before intervention) * Use of laxatives or pre- or probiotic supplements in the previous 4 weeks before intervention * Child is currently involved or will be involved in another clinical or food study

Design outcomes

Primary

MeasureTime frameDescription
Stool consistency4 weeksAssessed by the parents in a continuous daily bowel diary over the study period

Secondary

MeasureTime frameDescription
Stool colour4 weeksAssessed by the parents in a continuous daily bowel diary over the study period
Stool amount4 weeksAssessed by the parents in a continuous daily bowel diary over the study period
Sleep4 weeksChange in sleep behavior assessed by parental questionnaire (Brief Infant Sleep Questionnaire) at the beginning and end of the trial
Stool pH4 weekschange in stool pH over a four week period
Stool frequency4 weeksAssessed by daily parental reporting
Tolerance and acceptability4 weeksTolerance and acceptability of the study products assessed by customized parental questionnaire at the end of the trial
Body weight4 weekschanges in body weight (kg) assessed by an investigator
Body height4 weekschanges in body height (m) assessed by an investigator
Faecal Microbiota4 weeksStool samples will be analysed by appropriate molecular biological methods like 16S rRNA gene sequencing to gain insight into the composition of the gut microbiota.
stool short-chain fatty acids4 weekschange in amount and relative distribution of short-chain fatty acids in stool over a four week period

Countries

Spain

Contacts

Primary ContactStephan Theis, PhD
stephan.theis@beneo.com+49 6359 803 287

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026