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OpenTrials
Completed

NCT Number: NCT01542320

Effect of Probiotic Supplementation on Immune Function in Healthy Infants

The purpose of this study is to understand how a probiotic might change the immune response of healthy infants.

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Key information

Age range

6 week–32 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Emory Children's Center

Atlanta, Georgia, 30322, United States

About this study

PROBLEM OF INTEREST: Lactic acid bacteria known as probiotics have been given to children and adults to prevent and treat gastrointestinal infections and to maintain intestinal health. This pilot study will collect information (biomarkers) of inflammation and immune response from healthy infants.

HOW THE PROBLEM WILL BE STUDIED: The investigators will give an active Lactobacillus-containing probiotic or an inactive placebo without Lactobacillus to 38 healthy infants in the metropolitan Atlanta area from 2 weeks before until 2 weeks after they complete their rotavirus vaccine series. Half will be assigned to receive the active probiotic, half to receive the placebo. Neither the investigators nor the parent/ guardian of the study subject will know whether their infant is receiving the probiotic or placebo. A teaspoon of blood and a stool sample will be collected from each infant before they start taking the active probiotic or placebo and 2 weeks after they complete their rotavirus vaccine series. Each infant will receive the probiotic or placebo product for 2 weeks before starting their rotavirus vaccine series until 2 weeks after they complete their rotavirus vaccine series. The blood and stool samples will be examined for levels of inflammatory markers and measures of immune response. The stool samples may be stored for the later study of probiotic bacteria as well as for other bacteria and viruses. These results will help to determine if this Lactobacillus containing probiotic has an effect on immune response and inflammation in healthy infants.

HOW RESEARCH WILL ADVANCE SCIENTIFIC KNOWLEDGE AND HUMAN HEALTH: This study will provide new information about the impact of giving a Lactobacillus-containing probiotic supplement to healthy infants. CURRENT STANDARD OF CARE: The current standard of care is for infants to receive a probiotic at the discretion of their caregiver. By studying probiotic administration in a controlled way with a fixed dose schedule and a well categorized probiotic, and measuring blood and stool markers, the investigators hope to better understand the impact of a probiotic on immune response and inflammation.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy infant
  • Eligible for rotavirus immunization series
  • No recognized immunodeficiency
  • Ability to comply with study procedures

Exclusion criteria

  • Ineligible for rotavirus immunization series
  • Recognized immunodeficiency
  • Inability to comply with study procedures

Treatment and study plan

Lactobacillus reuteri DSM 17938

Dietary Supplement

1 x 10e8 colony forming units in 5 drops (0.17ml)daily from study enrollment to study conclusion. Duration based on rotavirus vaccine administration.

Other names: BioGaia infant drops

Placebo

Other

Solution without active Lactobacillus reuteri

Other names: Inactive solution

Primary outcomes

  1. Biomarkers of immune response

    Time frame: Between 18 and 32 weeks of age

Sponsors and collaborators

Lead sponsor

Emory University

Other

Collaborators

  • The Gerber Foundation

Registry information

Official study title

Application of Therapeutic Microbiology to Improve Immunogenicity

Acronym: ProBoost

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Mar 2, 2012
Registry last updated
Mar 6, 2015

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.

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