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 @ 10:06 PM
Ignite Modification Date:
2025-12-24 @ 10:06 PM
NCT ID:
NCT07110935
Eligibility Criteria:
Inclusion Criteria:
* Women who have vaginal delivery of singleton baby and are seen within 48hours of childbirth
* Women with mild and moderate anaemia
* Women who gave their consent to participate in the study.
Exclusion Criteria:
* Women with severe anaemia
* Women with multiple pregnancy
* Women with genotype HbSS
* Women with HIV infection
* Women who delivered by caesarean section
* Women with co-morbidity like hypertensive disorders, renal pathology
* Women who decline consent after adequate counseling.
* Previous and current history of adverse reaction to iron dextran
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
39 Years
Study:
NCT07110935
Study Brief:
Protocol Section:
NCT07110935