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Clinical Trials/NCT01603719
NCT01603719
Completed
N/A

Safety and Efficacy of an Infant Starter Formula With Prebiotics (GOS) and a Higher Content of Beta-palmitate on Stool Characteristics, Food Tolerance, Calcium Uptake, and Incidence of Infectious Disease in the First Year of Life

Waldkrankenhaus Protestant Hospital, Spandau1 site in 1 country128 target enrollmentAugust 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Infections
Sponsor
Waldkrankenhaus Protestant Hospital, Spandau
Enrollment
128
Locations
1
Primary Endpoint
number of gastrointestinal infections
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this clinical trial is to evaluate the effect of a new infant starter formula with added prebiotics (GOS) and with a fat blend rich in beta-palmitate.

Detailed Description

An experimental infant formula with added prebiotics (GOS) and with a higher content of palmitic acid esterified in beta-position is to be tested in a double-blinded randomized controlled trial. The addition of prebiotics to an infant formula should favor growth of a beneficial bifidogenic intestinal flora and have positive effects on immunity, promote softer stool formation and short chain fatty acid content in the stools. Higher proportion of beta-palmitic acid esterified in 2nd position of the triglyceride should reduce formation of fatty acid-calcium soaps in the stools and promote calcium and fat absorption in the gut, therfor reduce symptoms of constipation and colics.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
January 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Waldkrankenhaus Protestant Hospital, Spandau
Responsible Party
Principal Investigator
Principal Investigator

Antonia Nomayo, MD

MD

Waldkrankenhaus Protestant Hospital, Spandau

Eligibility Criteria

Inclusion Criteria

  • healthy term neonates
  • gestational age 37 to 42 weeks
  • birth weight 10th to 90th percentile (Voigt reference)
  • infants being exclusively formula-fed at enrollment

Exclusion Criteria

  • infants with high risk of atopic disease due to family history
  • congenital disorder or syndrome with need for special diet / impairment of growth
  • antibiotic medication prior to enrollment

Outcomes

Primary Outcomes

number of gastrointestinal infections

Time Frame: within first year of life

Secondary Outcomes

  • number of infectious episodes (gastrointestinal, respiratory, fever episodes)(within first year of life)
  • symptoms of food intolerance, constipation, colics(after 6 weeks, 12 weeks intervention)
  • atopic manifestation(within 1st year of life)
  • anthropometric parameters (gain in weight, length, head circumference)(after 6 weeks, after 12 weeks intervention)
  • proportion of bifidobacteria on total stool bacteria(after 6 and 12 weeks intervention)
  • stool biochemistry (calcium-fatty acid soaps, short chain fatty acids content in the stools)(after 6 weeks, 12 weeks intervention)
  • calcium absorption(after 6 weeks, 12 weeks intervention)
  • erythrocytes´ fatty acid profile(after 6 weeks intervention)

Study Sites (1)

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