Synbiotics and Growth

Infants Growth Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01886898
• Other study ID #: 05.23.INF
• Status: Completed
• Phase: Phase 3
• First received: June 24, 2013
• Last updated: June 25, 2013
• Start date: June 2007
• Est. completion date: October 2009

Study information

• Verified date: June 2013
• Source: Nestlé
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 311
• Est. completion date: October 2009
• Est. primary completion date: February 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: N/A to 14 Days

Eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)

Related Conditions & MeSH terms

• Infants Growth

Intervention

Other:
• Infant formula
infant formula
• Breastfeeding

Locations

Country	Name	City	State
Italy	Istituto di Ostetricia e Genecologia	Palermo

Sponsors (1)

Lead Sponsor	Collaborator
Nestlé

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	mean weight gain (g/day)		over 16 weeks	No
Secondary	length (cm), head circumference (cm)		over 1 year	No
Secondary	• digestive tolerance (stool characteristics and frequency, vomiting, spitting up, frequency of colic)		over 4 months	No