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Protocol for a multicenter, double-blinded placebo-controlled randomized controlled trial comparing intravenous ferric derisomaltose to oral ferrous sulfate for the treatment of iron deficiency anemia in pregnancy: The IVIDA2 trial.

Authors :
Lewkowitz, Adam K.
Stout, Molly J.
Carter, Ebony B.
Ware, Crystal F.
Jackson, Tracy L.
D'Sa, Viren
Deoni, Sean
Odibo, Anthony O.
Gopalakrishnan, Riley
Liu, Jingxia
Rouse, Dwight J.
Auerbach, Michael
Tuuli, Methodius G.
Source :
Contemporary Clinical Trials. Dec2022, Vol. 123, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Iron deficiency anemia (IDA) is common during pregnancy and associated with adverse maternal and neonatal outcomes. Treatment with iron supplementation is recommended during pregnancy, but the optimal delivery route is unclear. Oral iron risks has high risk of gastrointestinal side effects and low absorption. Intravenous iron is infused directly but is expensive. The American College of Obstetricians and Gynecologists currently recommends oral iron to treat IDA in pregnancy with intravenous iron reserved as second-line therapy, if needed. This approach is associated with persistent anemia, increasing the risk of peripartum blood transfusion. We aim to provide data on optimal route of iron repletion for IDA in pregnancy. In IVIDA2, a double-blind, placebo controlled, multicenter randomized trial in the United States, 746 pregnant people with moderate-to-severe IDA (hemoglobin <10 g/dL and ferritin <30 ng/mL) at 24–28 weeks' gestation will be randomized 1:1 to either a single 1000 mg dose of intravenous ferric derisomaltose and oral placebo (1–3 times daily) or a single placebo infusion with 1–3 times daily 325 mg ferrous sulfate (65 mg elemental iron) tablet. The primary outcome is peripartum blood transfusion (blood transfusion from delivery to 7 days postpartum). Secondary outcomes include adverse medication reactions, maternal and neonatal hematologic indices, and offspring neurodevelopment. A central ethical review board—Advarra—granted ethical approval (Pro00060930). Participating centers—Women & Infants Hospital of Rhode Island, University of Michigan Medical Center, Washington University School of Ethics and dissemination: A central ethical review board—Advarra—granted ethical approval (Pro00060930). Participating centers—Women & Infants Hospital of Rhode Island, University of Michigan Medical Center, Washington University School of. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15517144
Volume :
123
Database :
Academic Search Index
Journal :
Contemporary Clinical Trials
Publication Type :
Academic Journal
Accession number :
161009708
Full Text :
https://doi.org/10.1016/j.cct.2022.106992