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 @ 2:23 AM
Ignite Modification Date:
2025-12-25 @ 2:23 AM
NCT ID:
NCT03830034
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women at 14 -18 weeks of gestation calculated from the first day of their last menstrual period and confirmed or modified by ultrasound
* Hemoglobin level 8-10.5 g/dL
* Serum ferritin\<15µg/L
Exclusion Criteria:
* The presence of anemia from causes other than iron deficiency(e.g: Folat deficiency anemia,Vitamin B12 deficiency, ect…).
* Multiple gestations
* The presence of clinical and/or laboratory evidence of hepatic, renal, hematological or cardiovascular disease
* Patients with known gastritis
* History of mal-absorption syndrome
* Those with known hypersensitivity to iron preparations
* Those under current iron supplementation
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT03830034
Study Brief:
Protocol Section:
NCT03830034