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

RecruitingNAAges 2 Hours - anyAllTurku University Hospital
NCT06974994 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: Pregnant women (n=125) and their newborn children who receive antibiotic treatment at delivery. Exclusion Criteria: * Chorioamnionitis * Pre-eclampsia and hepatogestosis * Suspected malformation or serious condition of the foetus and neonates * Serious infection or other conditions not permitting breast milk feeding
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What it tests

  • Synbiotic Supplement
  • Placebo
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Where

1 site
Department of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku
Turku, Finland
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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