Overview

Assessment of Iron Absorption From Aspergillus Oryzae

Status:
Completed
Trial end date:
2016-06-04
Target enrollment:
0
Participant gender:
Female
Summary
The objective of this study was to compare the absorption of a new iron product, iron enriched Aspergillus oryzae to ferrous sulfate in humans using a double stable-isotope technique.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Iowa State University
Treatments:
Iron
Criteria
Inclusion Criteria:

- Marginal iron status (Serum ferritin <30ug/L)

- BMI in the range 18.5-24.9 kg/m2

- Willing to discontinue vitamin and mineral supplements 2 weeks prior and during the
study

- Willing to consume stable iron isotope labelled supplement

- Willing to stop getting blood drawn 2 weeks prior to the study and during the study

- Willing to give multiple blood samples at beginning and end of study

Exclusion Criteria:

- Pregnant

- Lactating

- Smoker

- Anemic (hemoglobin < 120 g/L)

- Has gastro-intestinal disease/condition that can affect absorption

- Allergic to any of the meal components