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Clinical Trial Summary

Evaluate the extent to which treatment of iron deficiency anemia beyond 24-34 weeks' gestation of pregnancy with intravenous iron increases hemoglobin compared to oral iron. The investigators will test the hypothesis that pregnant women who are anemic in the second and third trimester are more likely to significantly increase their hemoglobin with intravenous iron as opposed to the usual standard of care, oral iron.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04253626
Study type Interventional
Source Stanford University
Contact
Status Active, not recruiting
Phase Phase 3
Start date January 21, 2021
Completion date July 2024

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