Iron Treatment for Young Children With Non-anemic Iron Deficiency (OptEC)
Non-anemic Iron Deficiency
About this trial
This is an interventional treatment trial for Non-anemic Iron Deficiency focused on measuring child development, screening, Non-anemic iron deficiency, primary care pediatrics, prevention and health promotion
Eligibility Criteria
Inclusion Criteria:
- Age between 18 and 36 months attending any well child visit
- Informed parental consent
Exclusion Criteria:
- Previously diagnosed: developmental disorder, genetic, chromosomal or syndromic condition, chronic medical condition, (with the exception of asthma and allergies), including chronic anemia, iron deficiency or recent oral iron supplementation or treatment
- Prematurity with a gestational age less than 35 weeks; low birth weight less than 2500 grams
- Attending the office for an acute illness, such as a viral illness, or other health concern other than well-child assessment
- Any contraindications to receiving elemental iron (i.e. NHP [natural health product], comparator or placebo)
- The use of any Natural Health Product containing the same medicinal ingredient(s) as the investigational product
- English not spoken to the child in the home or in a child care setting
Sites / Locations
- St. Michael's Hospital
- The Hospital for Sick Children
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Placebo Comparator
No Intervention
Active Comparator
Iron plus dietary counseling (Non-anemic iron deficiency)
Placebo plus dietary counseling (Non-anemic iron deficiency)
Iron sufficient
Iron deficiency anemia
From the screening cohort of it is anticipated that 25 children will have iron deficiency anemia and an equal number of randomly selected children with iron sufficiency (n=25) will be sampled. These children will be compared to the children with non-anemic iron deficiency.
From the screening cohort of it is anticipated that 25 children will have iron deficiency anemia and an equal number of randomly selected children with iron sufficiency (n=25) will be sampled. These children will be compared to the children with non-anemic iron deficiency.