Dietary Iron Requirements Study

This study aims to better understand how much iron adults in the US need in their diet. Current guidelines are based on studies in European populations, and this research will help update them for the US. You might be able to join if you are between 18 and 50 years old, male or a premenopausal female, and have either participated in a previous iron study or are willing to take a stable iron isotope (a safe, non-radioactive form of iron) and wait a year for it to settle in your body. You'll also need to avoid iron supplements and smoking during the study. The main goal is to measure the iron isotope levels in your blood after 12 weeks to see how your body uses iron. The study is currently unclear on its recruitment status, but plans to enroll 300 people.

Study design
This is an interventional study planning to enroll 300 participants. It uses a stable iron isotope to determine iron requirements.
What's involved
You will consume an oral stable iron isotope and undergo a one-year equilibration period. Then, you will be followed for 12 weeks, with blood collected every 4 weeks.
Compensation
Not stated in the trial record.
Follow-up
Your iron isotope composition in blood will be measured at 12 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07139821

Dietary Iron Requirements

Recruiting
NAAges 18–50Interventional
Pennington Biomedical Research Center
~300 participants
Updated 2026-04-29 on ClinicalTrials.gov
What's tested:Stable iron isotope

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Iron isotope composition in blood
Measured over 12 weeks
Iron Absorption

NCT07139821

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Cornell University

    Ithaca, New Yorkstudy coordinator listed

    Recruiting

  • LSU Pennington Biomedical Research Center

    Baton Rouge, Louisianastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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Eligibility criteria

Inclusion

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

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
  • Iron isotope composition in blood12 weeks

    Tracer-to-tracee rate in venous blood samples collected at multiple time points