Probiotic Supplementation in Optimizing Iron and Hematological Status Among Pregnant Females

Recruiting Phase 2 Interventional Study
Iron Deficiency (ID) Pregnancy
Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 45
Sex
Female
Trial phase
Phase 2
Study type
Interventional
Purpose
Prevention
Participants needed
250 (estimated)
Sponsor
University of Illinois at Chicago · Other
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About This Trial
Maternal iron deficiency (ID) and iron deficiency anemia (IDA) is associated with maternal and infant mortality, spontaneous preterm birth, maternal postpartum hemorrhage, and neurocognitive defects in the neonate. Therefore, preventing maternal IDA in at-risk women is critical. The standard approach to improving iron status in pregnancy (i.e., oral iron supplements) is suboptimal and gastrointest…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * singleton naturally conceived pregnancy; * at risk of IDA \[Hb 11.0 - 11.9 g/dL (first trimester) and Hb 10.5 - 11.5 g/dL (second trimester) based on new OB clinical complete blood count (CBC) results obtained from the EHR; * 18 - 45 years old; * 10-16 weeks GA; * fluency in E…
Contacts

Mary Dawn Koenig, PhD, RN, CNM

312-996-7982

marydh@uic.edu

CONTACT