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 @ 5:41 PM
Ignite Modification Date:
2025-12-24 @ 5:41 PM
NCT ID:
NCT05921968
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women with iron deficiency anemia.
* Microcytic hypochromic anemia, moderate anemia (Hb 8 to 9.9 g/dl) and S. Ferritin levels \<12 ng/dl as per WHO guidelines
* Gestational age: - 13-26 weeks.
* Singleton viable pregnancy
* Lastly, agreement to participate and sign the informed consent was a basic prerequisite
Exclusion Criteria:-
* Women with a history of anemia due to any other causes such as chronic blood loss, hemolytic anemia, and thalassemia (including thalassemia trait).
* Severe anemia \<7 g/dl requiring blood transfusion, bronchial asthma, clinical and/or laboratory evidence of hepatic, renal, hematologic or cardiovascular abnormalities.
* History of peptic ulcer.
* Hypersensitivity to iron preparations and treatment with any other iron preparation in the last one month before study entry.
* Suspected acute infection.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT05921968
Study Brief:
Protocol Section:
NCT05921968