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Recruiting Not applicable

The BEGIN Study Bifidobacterium Infantis to Newborns: Effects of Modulating the Gut Microbial Composition on Growth, Immune Function and Inflammatory Conditions - a Randomized Placebo-controlled Double-blinded Intervention Trial

NCT06452199 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2024-06-10
Last updated
2024-10-01

Condition(s) studied

HealthyHealthy Nutrition

Investigational drug(s) / intervention(s)

B. infantisPlacebo

B. infantis: 1000 newborn children are randomized 50/50 to receive either B. infanits or placebo in a dietary supplement, for daily oral administration in three weeks from 7 days of age.

Placebo: Identical looking placebo (without any probiotics/B. infantis) for double-blinded daily oral administration in three weeks from 7 days of age.

Study summary

The goal of The BEGIN Study, a randomized controlled double-blinded intervention trial, is to learn if probiotics, with Bifidobacterium longum subspecies infantis Bifin02 (B. infantis), given to healthy newborns can affect various health outcomes and to explore impacts of the infant gastrointestinal microbiome. The main questions it aims to answer are:

* Does B. infantis probiotics impact immune function and does it lower the number of bacterial infections and use of antibiotics?
* Does B. infantis probiotics impact overall health, development, growth and wellbeing?
* Does B. infantis probiotics impact inflammatory diseases, allergies and autoimmune diseases

Researchers will compare B. infantis probiotics to a placebo (a look-alike substance that contains no probiotic) to see if B. infantis colonization impact the human immunesystem and various clinical and biochemical health markers.

Participants (parents) will

* Orally administrate the B. infantis probiotic to their newborn child daily in three weeks from 7 days of age.
* Answer baseline and follow up questionnaires in a study app
* Take five stool samples from the child and one stool sample from the mother
* Collect a 4 week of passive dust sample at home (Electrostatic Dust fall Collector)
* Donate one dried bloodspot and one blood sample from their child

Eligibility

Sex
ALL
Min age
1 Day
Max age
7 Days
Healthy volunteers
Accepted
Inclusion Criteria: * Infants born at term (above gestational week 37) * Infants born in Region Midtjylland Denmark receiving a Danish CPR number. * Parents age is above 18 * At least one parent holds a smartphone (for study app) and is able to fill out Danish questionaries * Both legal parents are willing and able to provide written informed consent prior to participation, regarding both themselves and their future child. Exclusion Criteria: * Multiple pregnancy * Child diagnosed with immune deficiency, renal, gastrointestinal, hepatic, or endocrine diseases * Parents expecting to give other probiotics

Primary outcome measure(s)

  • Prescriptions of antibiotics — First assessment at 1 year and up to 18 years follow-up
    Number of prescriptions of antibiotics among participants, as a measure of bacterial infections.

Trial sites (2)

FacilityCityRegionStatus
Regional Hospital Gødstrup Herning Central Jutland Recruiting
Regional Hospital Horsens Horsens Central Jutland Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06452199 on ClinicalTrials.gov ↗ ← All trials in Denmark