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Growth of Infants Fed With BabyNes System

NCT01585142 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2015-01-16

No results posted yet for this study

Summary

The purpose of this study is to assess the growth of infants fed with BabyNes System, compared to the World Health Organization Reference, during the first four months of life.

Conditions

  • Dietary Modification

Interventions

OTHER

Test formula

Infant Formulas in powder in single-serve capsules (with a machine for dispensing, four consecutive formulas with customized composition

Sponsors & Collaborators

  • Société des Produits Nestlé (SPN)

    lead INDUSTRY

Principal Investigators

  • Johannes Spalinger, Dr med. · Pädiatrische Gastroenterologie und Hepatologie Kinderspital

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Max Age
14 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01585142 on ClinicalTrials.gov