Monoferric for Prenatal Iron Deficiency

Recruiting now · Early Phase 1

Conditions studied: Obstetric Labor Complications

In brief

A prospective observational study of pregnant women with iron deficiency anemia and oral iron intolerance or advanced gestational age.

Key facts

Study ID

NCT05763043

Run by

Oregon Health and Science University

People needed

80

Starts

2024-01-18

Expected to finish

2028-10-01

Last updated by the study team

2024-09-19

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Participants 18 years of age or older between 14 to 42 weeks gestation who are deemed appropriate for IV iron by their treating provider as part of their standard of care treatment.
• Iron deficiency anemia, defined as second or third trimester (14 weeks or more) hemoglobin less than or equal to 10.5 g/dL or less than or equal to11 g/dL, respectively, and ferritin less than 50 μg/L
• Experience intolerance to oral iron or are greater than 28 weeks gestation
• Willing to participate in the study

You may not qualify if…

• Known infectious, inflammatory, or malignant conditions that may confound iron repletion and outcome analysis
• Prior IV iron intolerance or hypersensitivity reaction

Where it is running

• Oregon Health & Science Univerity — Portland, Oregon, United States (enrolling)

Full record on ClinicalTrials.gov

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