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Digestive Tolerance of Slightly Hydrolyzed Starter Infant Formula With Probiotics

Tolerance of a Slightly Hydrolyzed Starter Formula Containing Probiotics

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01036243
Enrollment
480
Registered
2009-12-21
Start date
2009-12-31
Completion date
2012-04-30
Last updated
2012-06-22

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

Conditions

Infant Nutrition

Keywords

digestive tolerance, night sleep, crying, growth

Brief summary

To demonstrate that infants have improved gut comfort when fed a slightly hydrolyzed starter formula containing probiotics compared to infants fed a control hydrolyzed and referenced non-hydrolyzed formula.

Detailed description

Infants often experience undesirable gastrointestinal effects, such as constipation, flatulence. These symptoms are often perceived by the parents as being related to the diet (formula) the baby is consuming. In another hand, infantile colic or fussing/crying is one of the most commonly encountered problems within the first three months of life. The etiology of the disorder remains unknown however, three main theories have been proposed to explain its origin: (i) psychological: due to inadequate mother-infant interaction (ii) gastrointestinal: such as hypertonicity and immaturity of the GI tract and Dietary factors that may influence the stool pattern in formula fed infants are (iii) allergic: due to a reaction against cow's milk protein or other food constituents. e.g. the protein source, the iron content, hydrolyzation of the protein, or the fat source. It has been reported that infants receiving a casein predominant formula had less unformed stools than those receiving a whey predominant formula. Hydrolysation of protein resulted in reduced gastro-intestinal transit time and some studies using extensively hydrolyzed protein formula have shown more liquid stools. A reduction of crying hours was also described in infant receiving an hydrolyzed formula. Some probiotics were reported with potential benefit on the gut comfort.

Interventions

DIETARY_SUPPLEMENTtest formula 1

hydrolyzed formula with probiotics

DIETARY_SUPPLEMENTtest formula 2

acidified hydrolyzed formula

DIETARY_SUPPLEMENTtest formula 3

hydrolyzed formula without probiotics

DIETARY_SUPPLEMENTreference formula

standard infant formula

Sponsors

Chulalongkorn University
CollaboratorOTHER
Société des Produits Nestlé (SPN)
Lead SponsorINDUSTRY

Study design

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

Eligibility

Sex/Gender
ALL
Age
11 Days to 30 Days
Healthy volunteers
Yes

Inclusion criteria

* Healthy infants, 0-1 month old at point of enrollment * Birth weight \< 2500g and \> 4500g * Gestational age \< 37 weeks and \> 42 weeks * Infants who cannot be breastfed because of the maternal status * Willing to exclusively consume the assigned study formula with whey protein * Are likely to be compliant * Mother/caregiver demonstrates an understanding of the given information and ability to record the requested data

Exclusion criteria

* Congenital illness or malformation * Significant pre-natal and/or post-natal disease * Receiving systemic antibiotic treatment at time of enrolment * Infant with symptoms of allergy to cow's milk * Infant's family cannot be expected to comply with treatment (feeding regimen) * Subjects who cannot be expected to comply with treatment * Currently participating or having participated in another clinical trial during the last month

Design outcomes

Primary

MeasureTime frame
incidence of crying/fussing from 1 to 3 months.3 months

Secondary

MeasureTime frame
growth and night sleep6 months

Countries

Thailand

Outcome results

None listed

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