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Bioavailability of Iron From Savoury Food Product

Assessment of the Bioavailability of Iron in Iron Fortified Savoury Food Product in Healthy Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02280915
Enrollment
24
Registered
2014-11-03
Start date
2014-10-31
Completion date
2015-03-31
Last updated
2015-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy, Iron Deficiency

Keywords

female, subjects

Brief summary

The study is designed to assess the bioavailability of iron from 4 different iron fortified savoury food products

Interventions

OTHERSavoury food product

Sponsors

Unilever R&D
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Healthy female subjects; * Age \> 18 and \< 40 years at screening; * Body weight \<65 kg; * Apparently healthy: no medical conditions which might affect study measurements (judged by study physician); * With iron deficiency (Serum ferritin \<15µg/L); * Currently not smoking and being a non-smoker for at least six months and no reported use of any nicotine containing products in the six months preceding the study and during the study itself; * Willing and able to participate in the study; Having given a written informed consent.

Exclusion criteria

* Blood donation or significant blood loss over the past 6 months; * Reported use of any medically- or self-prescribed diet; * Use of medication (except oral contraceptives) * Use of vitamin or mineral supplements and unwillingness to discontinue their use two weeks prior the study and during the study; * Is pregnant or will be planning pregnancy during the study period; * Is lactating or has been lactating in the 6 weeks before pre-study investigation and/or during the study period; * Known gastrointestinal or metabolic disorders; * Participation in another clinical trial during the last 30 days prior to the beginning of the study.

Design outcomes

Primary

MeasureTime frameDescription
To assess the absolute bioavailability of iron from 4 different iron fortified savoury food products15 daysAmounts of Fe isotopic label present in the blood 14 days after administration of the fortified savoury food product will be calculated based on measured shifts in the iron isotope ratios in the blood samples (Day 15) compared to baseline and the amount of iron circulating in the body

Secondary

MeasureTime frameDescription
To assess the relative bioavailability of iron from iron fortified savoury food products15 daysThe absolute bioavailability results of each of the iron fortified savoury products as obtained under the primary objective will be compared with each other

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026