Skip to main content
OpenTrials
Completed

NCT Number: NCT01886898

Synbiotics and Growth

The primary objective of the trial is to assess the growth of the infants enrolled into the study. Other parameters to be measured include microbiota balance and certain blood biochemical values. In addition the infants' digestive tolerance of the formulae and frequency of morbidity will be investigated.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

Up to 14 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Istituto di Ostetricia e Genecologia

Palermo, 90127, Italy

About this study

The infants will be recruited between birth and 14 days of life and will start on the allocated study formula as soon as they are enrolled. In practice this will tend to be immediately after birth. The treatment period, in terms of data necessary for the primary outcome, will be until they reach 16 weeks old. Growth and other measurements will be collected on five separate occasions during this period, ie 2, 4, 8, 12 and 16 weeks of life. Although the study intervention formally ends at 16 weeks, it will be useful to have a follow up visit at 26 weeks to collect further data on the gut microflora in the sub-group of infants who have already provided a stool sample at 8 weeks. This follow-up visit will be of benefit to the subject as they receive a weight check and clinical examination by a paediatrician and will be offered to all subjects (no invasive procedures will be carried out).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy new-born infant
  • Infant is less14 days old on day of enrollment
  • Birthweight between 2500g and 4500g
  • Gestational age over 37 weeks
  • Singleton birth
  • Infant's mother, before the 14th day of the child's life, has elected not to breastfeed
  • Infant randomized in to a treatment group can expected to be exclusively fed the formula from enrolment until 16 weeks old
  • Having obtained his/her legal representative's informed consent

Exclusion criteria

  • Currently participating in another clinical trial
  • Congenital illness or malformation that may affect normal growth
  • Significant pre-natal and/or post-natal disease
  • Re-hospitalisation for more than 2 days in the first 14 days of life. (Exceptionally, infants re-hospitalized because of jaundice may be enrolled in the study).
  • Receiving antibiotic treatment at time of enrolment or in the 5 previous days.
  • Receiving infant formula containing probiotics and/or prebiotics at the time of enrolment

Treatment and study plan

Infant Formula

Other

infant formula

breastfeeding

Other

Primary outcomes

  1. mean weight gain (g/day)

    Time frame: over 16 weeks

Secondary outcomes

  1. length (cm), head circumference (cm)

    Time frame: over 1 year

  2. • digestive tolerance (stool characteristics and frequency, vomiting, spitting up, frequency of colic)

    Time frame: over 4 months

Sponsors and collaborators

Lead sponsor

Société des Produits Nestlé (SPN)

Industry

Registry information

Official study title

Growth of Infants Fed Starter Formula Containing Oligo-saccharides and the Probiotics Bifidobacterium & Lactobacillus

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Jun 26, 2013
Registry last updated
Jun 26, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.