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Study identifier: NCT06974994 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Resilience to Antibiotic-induced Obesogenic Microbiota: Discovering Mechanism of Microbiota Modulation

Condition: Healthy Newborn Infants  ·  Sponsor: Turku University Hospital

PhaseNA
Planned participants125
Who can joinAll sexes, 2 Hours to no upper limit
Healthy volunteersNo

About this study

The aim is to study whether the microbiota of children who are exposed to antibiotics at birth could be modified by synbiotic supplement and thereby reduce the risk of obesity, chronic diseases and respiratory tract infections. A total of 125 mother-child pairs will be recruited in this randomized, double-blind, placebo-controlled study. Infants are randomized to receive either a synbiotic supplement or a placebo for 2 months, after which their growth and morbidity will be monitored at the research clinic for 2 years.

This description comes directly from the study's public registry record.

Talk to the study team

Paula Tähtinen, MD, PhD  ·  +358-2-3130746  ·  paula.tahtinen@utu.fi

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Paediatrics and Adolescent Medicine, Turku University Hospital and University of TurkuTurku, Valitse Maakunta., FinlandRecruiting

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Source record: clinicaltrials.gov/study/NCT06974994