Intravenous Versus Oral Iron for Treating Iron-Deficiency Anemia in Pregnancy
Launched by WOMEN AND INFANTS HOSPITAL OF RHODE ISLAND · Jul 14, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the best way to treat iron-deficiency anemia in pregnant women. Iron deficiency anemia means that a person does not have enough iron in their body, which is crucial for making healthy red blood cells. In this trial, researchers are comparing two methods of treatment: intravenous (IV) iron, which is given through a vein, and oral iron, which is taken by mouth. The goal is to see whether IV iron is more effective and safer in helping mothers and their babies, especially in preventing severe complications during childbirth and improving the baby's development.
To participate in this study, women must be between 18 and 45 years old, pregnant with a single baby, and diagnosed with moderate to severe iron-deficiency anemia. They should be between 13 to 30 weeks along in their pregnancy and plan to give birth at a participating hospital. Participants can expect to receive either IV iron or oral iron and will be closely monitored throughout the trial. This study is currently recruiting participants, and it’s important for interested individuals to discuss their eligibility and any questions with their healthcare provider.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Pregnant women between the ages of 18-45
- • Singleton gestation
- • Iron-deficiency anemia (serum ferritin \<30ng/mL and Hb\<11 g/dL)
- • At 13-30 weeks gestation
- • Plan to deliver at participating hospital
- Exclusion Criteria:
- • Non-iron-deficiency anemia e.g thalassemia, sickle cell disease, B12 or folate deficiency, hypersplenism.
- • Malabsorptive syndrome, inflammatory bowel disease, gastric bypass, or sensitivity to oral or IV iron
- • Multiple gestation
- • Inability or unwillingness to provide informed consent
- • Inability to communicate with members of the study team, despite the presence of an interpreter
- • Planned delivery at a non-study affiliated hospital
About Women And Infants Hospital Of Rhode Island
Women & Infants Hospital of Rhode Island is a leading healthcare facility dedicated to the comprehensive care of women and infants, with a strong focus on research and clinical trials aimed at advancing maternal and neonatal health. As a prominent academic medical center affiliated with Brown University, the hospital leverages its expertise in obstetrics, gynecology, and pediatrics to conduct innovative clinical trials that address critical health issues facing women and infants. Committed to improving patient outcomes through evidence-based practices, Women & Infants Hospital fosters a collaborative environment that encourages the integration of cutting-edge research into clinical care, ultimately enhancing the quality of life for its patients and the broader community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Salt Lake City, Utah, United States
Providence, Rhode Island, United States
Providence, Rhode Island, United States
Ann Arbor, Michigan, United States
Saint Louis, Missouri, United States
Birmingham, Alabama, United States
Miami, Florida, United States
Portland, Oregon, United States
Miami, Florida, United States
Patients applied
Trial Officials
Methodius Tuuli, MD, MPH, MBA
Principal Investigator
Women and Infants Hospital of Rhode Island
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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