Iron Absorption and Requirements in Pregnancy and Lactation

Recruiting Observational Study
Iron Requirements Pregnancy Lactation Infancy Iron Absorption
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 45
Sex
Female
Study type
Observational
Participants needed
250 (estimated)
Sponsor
University of Oxford · Other
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About This Trial
Iron requirements increase significantly during pregnancy. Current recommendations for iron intake in pregnant and lactating women (PLW) are mainly based on factorial estimates and extrapolated from non-PLW. High-quality quantitative data on iron requirements in PLW are lacking, particularly in Sub- Saharan Africa where anaemia and infections are common. The primary objective of this study is to …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Providing consent to the informed consent form * Participation in a previous stable isotope absorption study and having received an oral dose of 15 mg 57Fe at least 12 months prior to the date of inclusion in the study * Positive pregnancy test and gestational age \<10 weeks b…
Contacts

Nicole Stoffel, PhD

+41446328393

nicole.stoffel@rdm.ox.ac.uk

CONTACT

Joyce Wali, BSc

+254704862877

stellawali507@gmail.com

CONTACT