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Study identifier: NCT06219525 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Higher and Standard Doses of Enteral Zinc Supplementation in Very Preterm Infants

Condition: Very Preterm Infants · Zinc Deficiency  ·  Sponsor: Prince of Songkla University

PhaseNA
Planned participants120
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The goal of this randomized clinical trial is to compare the effect of higher (10 mg per day) versus standard (1 mg per day) doses of zinc supplementation The main questions it aims to answer are: * Growth velocities and delta z-scores during the date of start intervention until the end of the time interval (at least 2 weeks of intervention on date of 44 weeks of postmenstrual age or discharge whichever came first) in very preterm infants with a birthweight less than1800 grams. * Growth and neurodevelopment at 24 months postnatal age

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

Talk to the study team

Anucha Thatrimontrichai, MD  ·  +66 954300690  ·  tanucha@medicine.psu.ac.th

Boonwiroj Jitwilertrat, MD  ·  +66 914953851  ·  Boonwiroj@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Songklanagarind Hospital, Prince of Songkla UniversityHat Yai, Changwat Songkhla, ThailandRecruiting

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Source record: clinicaltrials.gov/study/NCT06219525