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Efficacy and Tolerance of a Follow-On Formula Fed to Children From 36-48 Months of Age

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Mead Johnson Nutrition

Status

Completed

Conditions

Acute Respiratory Infection
Diarrheal Disease

Treatments

Dietary Supplement: Cow's milk
Dietary Supplement: Follow-On Formula

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01488435
6012 (Other Identifier)

Details and patient eligibility

About

The purpose is to determine if the consumption of study product has an effect on acute respiratory infections and/or diarrheal disease.

Enrollment

310 patients

Sex

All

Ages

36 to 48 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Child 36-48 months of age
  • Child is currently attending a daycare and has attended for 6 months or less
  • Has consumed cow's milk or a cow's milk-based beverage during the 48 hours prior to randomization
  • Signed informed consent

Exclusion criteria

  • Child who received any food product or supplement containing probiotics or prebiotics in the 15 days prior to randomization
  • Child with allergy to gluten or serious concurrent illness that will interfere in the general management of the child
  • Child with diarrhea or acute respiratory infection during the 48 hours prior to randomization
  • Child's z-score of weight for height < -3 according to World Health Organization criteria

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

310 participants in 2 patient groups, including a placebo group

Cow's Milk
Placebo Comparator group
Description:
Powdered whole cow's milk
Treatment:
Dietary Supplement: Cow's milk
Follow-On Formula
Experimental group
Description:
Powdered Follow-On Formula with added long-chain Polyunsaturated fatty acid, prebiotics, and polysaccharide
Treatment:
Dietary Supplement: Follow-On Formula

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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