Clinical Trials Logo

Clinical Trial Summary

The investigators will randomize women diagnosed with anemia in the mid-trimester of pregnancy to once or twice daily iron supplementation


Clinical Trial Description

Women defined as having iron deficiency anemia based on a low hemoglobin as defined by the American College of Obstetrics and Gynecology and a low serum ferritin, in the absence of hemoglobinopathy, will be randomized to ferrous sulfate 325mg PO daily or PO twice daily. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02839096
Study type Interventional
Source University of Missouri-Columbia
Contact Daniel Jackson
Phone 5734996041
Email jacksondl@health.missouri.edu
Status Recruiting
Phase N/A
Start date June 2016
Completion date December 2019

See also
  Status Clinical Trial Phase
Completed NCT03922087 - No-worry Baby Project
Completed NCT03175042 - Non-invasive Spot Hemoglobin Measurement in the Outpatient Obstetric Clinic
Terminated NCT01193192 - A Retrospective Analysis of Neevo® and NeevoDHA® Compared to a Standard Prenatal Vitamin in Anemia During Pregnancy N/A
Completed NCT01062958 - A Retrospective Analysis of Neevo®/Neevo®DHA Compared to a Standard Prenatal Vitamin in Anemia During Pregnancy N/A
Completed NCT03689218 - Evidence Generation Related to Stunting Prevention in Balochistan N/A
Withdrawn NCT03564756 - Effect of Ascorbic Acid Supplementation in Pregnancy on Anemia (AAA) N/A