Plant-Derived heme iron: a new way to fight iron deficiency?
NCT ID NCT07143890
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how well iron-deficient women absorb iron from two plant-based sources—iron chlorophyllin and soy hemoglobin—compared to standard ferrous sulfate and animal-based heme iron. Forty-five women with low iron stores but not anemic took each type of iron in water or maize porridge. Researchers measured iron absorption in blood after 14 days to see if plant heme could be a good alternative for fortifying foods.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- iron chlorophyllin, soy hemoglobin, ferrous sulfate, porcine hemoglobin
- What this could lead to
- If plant-derived heme iron is absorbed well, it could lead to better iron fortification in foods, helping prevent iron deficiency without relying on animal sources.
- What could go wrong
- This is a small, completed experimental study in 45 women, not a treatment trial. Results may not apply to men, children, or people with anemia, and plant heme may not work as well in real-world diets.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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45 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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May 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Serum ferritin \< 45 µg/L (iron depleted) * Body weight \< 70 kg * Body mass index 18,5 - 24,9 kg/m2 (normal weight) Exclusion Criteria: * Hb \< 120 g/L (anemia) * CRP \> 5 µg/L (inflammation) * Strict vegan and vegetarians * Any metabolic, gastrointestinal kidney or chronic disease * Consumption of mineral and vitamin supplements since screening and over the study period until last blood sample collection * Blood transfusion over the past 6 months * blood donation over the past 6 months * Significant blood loss (accident, surgery) over the past 6 months * Women who are pregnant or breast feeding * Smoker (\> 1 cigarette per week) * Continuous/long-term use of medication (except for contraceptives) * Therapeutic iron infusion over the past 6 months, * Known hypersensitivity or allergy to iron supplements, * Intention to become pregnant during the course of the studies, * Known or suspected non-compliance, drug or alcohol abuse, * Inability to follow the procedures of the studies, e.g. due to language problems, psychological disorders, dementia, etc. of the participant, * Participation in another study with investigational drug within the 30 days preceding and during the present studies, * Enrolment of the investigator, his/her family members, employees and other dependent persons
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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ETH Zurich, Laboratoy of Clinical Biopharmacy
Zurich, 8092, Switzerland
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