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Recruiting NCT06318858

NCT06318858 Daily and Weekly Iron Supplementation in Infants

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Clinical Trial Summary
NCT ID NCT06318858
Status Recruiting
Phase
Sponsor Mahidol University
Condition Anemia
Study Type INTERVENTIONAL
Enrollment 300 participants
Start Date 2023-03-15
Primary Completion 2024-08-14

Trial Parameters

Condition Anemia
Sponsor Mahidol University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 300
Sex ALL
Min Age 6 Months
Max Age 12 Months
Start Date 2023-03-15
Completion 2024-08-14
Interventions
Iron supplement

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Brief Summary

This study aims to compare the efficacy of daily iron supplementation and weekly iron supplementation in infants aged 6-12 months on the prevalence of anemia, hemoglobin level, and serum ferritin levels. Infants will be enrolled at 6 months and will be randomly assigned to receive either daily or weekly iron supplementation for the first 3 months and will be followed by weekly iron supplementation for another 3 months.

Eligibility Criteria

Inclusion Criteria: * Apparently healthy infant, aged 6 months ± 2 weeks * Having a birth weight between 2,500 and 4,000 grams * Being born full term (37 to 41 weeks of age + 6 days) * Having hemoglobin ≥ 10.5 g/dL * Being planned to breastfeed with complementary food and/or complementary foods with formula milk Exclusion Criteria: * Infants with chronic illnesses or thalassemia clinical signs such as anemia, enlarged liver, or spleen (if parental history suggests the child is at risk of developing a thalassemia disease that may not show clinical symptoms) * Previously or currently taking an iron supplement

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