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:
2026-03-26 @ 3:18 PM
Ignite Modification Date:
2026-03-26 @ 3:18 PM
NCT ID:
NCT07356258
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women aged 18-50
* Indication for oral iron treatment as determined by the treating physician, in accordance with standard clinical practice
* Baseline iron store levels measured prior to initiation of oral iron therapy
Exclusion Criteria:
* Women taking ferrous sulfate 80 mg Tardiferon
* Gastrointestinal diseases such as colitis
* Women who received intravenous iron during pregnancy
* Women who received blood transfusions during pregnancy
* Women with anemia due to causes other than iron deficiency
* History of bariatric surgery
* Allergy to ferrous sulfate
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT07356258
Study Brief:
Protocol Section:
NCT07356258