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:
2025-12-25 @ 2:22 AM
Ignite Modification Date:
2025-12-25 @ 2:22 AM
NCT ID:
NCT03225534
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women aged 18 years and older (19 in Vancouver) 2. Residence in reasonable proximity to the delivery hospital 3. Able to read, write, and speak English 4. Willing to provide informed consent 5. Willing to consent to cord blood collection for the study 6. Planning to give birth at a designated recruitment centre participating hospital 7. Infants born at or after 35 weeks 8. Able to provide address and telephone number and names and telephone numbers of two alternate contact individuals
Exclusion Criteria:
1. Children with major congenital abnormalities or respiratory distress syndrome (RDS)
2. Expectation of moving away from a recruitment area within year 1
3. Children of multiple births
4. Children resulting from in vitro fertilization
5. Children who will not spend at least 80% of nights in the index home
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
1 Day
Maximum Age:
18 Months
Study:
NCT03225534
Study Brief:
Protocol Section:
NCT03225534