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Microbiota composition in healthy termed infants consuming infant formulae with different fat blends.

Recruiting
Conditions
Microbiota modulation, absorption of fat and calcium, gut comfort, stool consistency
Registration Number
NL-OMON27114
Lead Sponsor
FrieslandCampina N.V.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
14
Inclusion Criteria

Full-term, healthy infants (born at gestational age =37 weeks).
- Appropriate for gestational age birthweight (i.e. 10th centile = Birth weight = 90th centile).
- Age at enrolment: between 9th-14th 16th week
- Exclusively formula fed infants at least two weeks before recruitment and during the entire intervention period.
- Parents willing and agreeing to initiate complementary feeding after the end of endpoint measurements, i.e. after the completion of the 5.5th month of age
- Parents willing to collect stools and fill in all study questionnaires and diaries during the entire intervention period
- Written informed consent

Exclusion Criteria

- Severe acquired or congenital diseases, mental or physical disorders, any symptoms of allergy (including cow¡¯s milk allergy).
- No parents or siblings with documented CMA allergy, diagnosed by a doctor.
- Use of probiotics, antibiotics or other medication that treats or causes GI symptoms and/or affect appetite at the time of screening or at any time throughout the study period (these infants will be considered as drop-outs).
- Use of medication(s) known or suspected to affect fat digestion, absorption and/or metabolism; nutritional supplements; suppositories; medication that may suppress or neutralize gastric acid secretion and gut mobility at the time of screening or at any time throughout the study period (these infants will be considered as drop-outs).
- Participation in another clinical trial.
- Any type of mixed feeding (i.e. combination of formula with breastfeeding in any proportion) and/or complementary feeding during the intervention.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Microbiota composition
Secondary Outcome Measures
NameTimeMethod
Fatty acids absorption, Calcium absorption and gut comfort
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