Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT07139821

Dietary Iron Requirements

Led by Pennington Biomedical Research Center · Updated on 2026-04-29

300

Participants Needed

2

Research Sites

172 weeks

Total Duration

On this page

Sponsors

P

Pennington Biomedical Research Center

Lead Sponsor

C

Cornell University

Collaborating Sponsor

AI-Summary

What this Trial 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.

CONDITIONS

Official Title

Dietary Iron Requirements

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Males and premenopausal females age 18-50 years
  • 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
Not Eligible

You will not qualify if you...

  • Females who are pregnant, lactating, or planning to become pregnant during the study period
  • Inability to provide informed consent and engage in consent procedures
  • Plans to relocate outside the study area

AI-Screening

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Trial Site Locations

Total: 2 locations

1

LSU Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States, 70808

Actively Recruiting

2

Cornell University

Ithaca, New York, United States, 14853

Actively Recruiting

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Research Team

S

Stephen Hennigar, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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