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Recruiting NCT06974994

NCT06974994 Resilience to Antibiotic-induced Obesogenic Microbiota: Discovering Mechanism of Microbiota Modulation

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Clinical Trial Summary
NCT ID NCT06974994
Status Recruiting
Phase —
Sponsor Turku University Hospital
Condition Healthy Newborn Infants
Study Type INTERVENTIONAL
Enrollment 125 participants
Start Date 2024-05-08
Primary Completion 2029-12

Eligibility & Interventions

Sex All sexes
Min Age 2 Hours
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Synbiotic SupplementPlacebo

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 125 participants in total. It began in 2024-05-08 with a primary completion date of 2029-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

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

Contact & Investigator

Central Contact

Paula Tähtinen, MD, PhD

✉ paula.tahtinen@utu.fi

📞 +358-2-3130746

Frequently Asked Questions

Who can join the NCT06974994 clinical trial?

This trial is open to participants of all sexes, aged 2 Hours or older, studying Healthy Newborn Infants. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06974994 currently recruiting?

Yes, NCT06974994 is actively recruiting participants. Contact the research team at paula.tahtinen@utu.fi for enrollment information.

Where is the NCT06974994 trial being conducted?

This trial is being conducted at Turku, Finland.

Who is sponsoring the NCT06974994 clinical trial?

NCT06974994 is sponsored by Turku University Hospital. The trial plans to enroll 125 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology