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.
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