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 @ 12:55 PM
Ignite Modification Date:
2025-12-24 @ 12:55 PM
NCT ID:
NCT05883761
Eligibility Criteria:
Surveillance component includes all deliveries/admissions as defined in study population description. For a subset of the population recruited for additional data collection:
Inclusion Criteria:
* women whose live or stillborn infant has birth defect as identified by a midwife or other clinician at the study hospital
* willing to provide informed consent
Exclusion Criteria:
* unable to provide informed consent
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT05883761
Study Brief:
Protocol Section:
NCT05883761