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:
2025-12-26 @ 11:46 AM
Ignite Modification Date:
2025-12-26 @ 11:46 AM
NCT ID:
NCT04235816
Eligibility Criteria:
Inclusion Criteria:
* Parents/guardians have signed the informed consent
* Permanent residence in the study area-health facility catchment area
* Without known allergies to or contraindications to macrolides
* Without known allergies to or contraindications to SP
* Agreement to complete the EPI scheme at the recruitment health facility
* Parents/guardians agree to participate
Exclusion Criteria:
* Residence outside the study area or planning to move out in the following 12 months from enrolment
* Known history of allergy or contraindications to macrolides and/or SP
* Known history of allergy or contraindications to SP
* With signs of any acute illness at the time of recruitment
* Participating in other intervention studies
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
6 Weeks
Maximum Age:
8 Weeks
Study:
NCT04235816
Study Brief:
Protocol Section:
NCT04235816