Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:05 PM
Ignite Modification Date:
2025-12-24 @ 4:05 PM
NCT ID:
NCT01481766
Eligibility Criteria:
Inclusion Criteria:
* Age between 12 and 40 months attending any well child visit
* Informed parental consent
Exclusion Criteria:
* developmental disorder
* genetic, chromosomal or syndromic condition
* chronic medical condition (with the exception of asthma and allergies)
* chronic anemia, iron deficiency, or recent oral iron supplementation or treatment
* prematurity, with a gestational age of less than 35 weeks
* low birth weight less than 2,500 g;
* attending the office for an acute illness, such as a viral illness, or other health concern other than for a well-child assessment
* any contraindications to receiving elemental iron
* the use of any natural health product containing the same medicinal ingredient(s) as the investigational product
* English is not spoken to the child in the home or in a child care setting
* CRP level ≥10 mg/L
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
12 Months
Maximum Age:
40 Months
Study:
NCT01481766
Study Brief:
Protocol Section:
NCT01481766