Dietary Iron Requirements
Pennington Biomedical Research Center · with Cornell University · NCT07139821
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–50 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 300
- US sites recruiting
- 2
- Study start
- February 6, 2026
- Record last updated
- April 29, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Dietary Reference Intakes (DRIs) for iron are based on a relatively small number of studies in European populations. This research study will determine iron needs in a representative sample of adults living in the US using the iron isotope dilution technique. Following administration and equilibration of a stable iron isotope, participants will be followed for a 12 week study period. Blood will be collected every 4 weeks and the isotopic composition will be determined. Results will help update dietary iron guidelines making sure they better match the specific needs of the US population.
Being studied: Stable iron isotope
Conditions: Iron Absorption
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Males and premenopausal females age 18-50 y
- Previously participated in an iron stable isotope study or willing to consume an oral stable iron isotope and undergo a one-year equilibration period
- Willing to refrain from iron-containing supplements for the duration of the study
- Willing to refrain from tobacco smoking for the duration of the study
- Have not donated blood 3 months prior to the start of the study and willing to refrain from donating blood for the duration of the study
- Willing to have blood stored for future use
- Able and willing to comply with study requirements and consent to participate
Exclusion Criteria
- Females: pregnant or lactating or plans to become pregnant during the study period
- Inability to provide informed consent and engage in informed consent procedures
- Plans to relocate outside the study area
Recruiting US locations
LSU Pennington Biomedical Research Center
Baton Rouge, LA 70808
Site contact: Stephen Hennigar, PhD · 225-763-2612 · stephen.hennigar@pbrc.edu
Cornell University
Ithaca, NY 14853
Site contact: Kimberly O'Brien, PhD · 607-255-3743 · koo4@cornell.edu
Study contacts (from the official record)
- Stephen Hennigar, PhD · 225-763-2612 · stephen.hennigar@pbrc.edu
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