Monoferric for Prenatal Iron Deficiency

Description

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

Conditions

Obstetric Labor Complications

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Study Overview

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Study Details

Study overview

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

Monoferric for Prenatal Iron Deficiency

Monoferric for Prenatal Iron Deficiency

Condition
Obstetric Labor Complications
Intervention / Treatment

-

Contacts and Locations

Portland

Oregon Health & Science Univerity, Portland, Oregon, United States, 97239

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

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

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Oregon Health and Science University,

Study Record Dates

2028-10