Actively Recruiting
Heme and Non-heme Iron Intakes, Gut Microbiota, and Influence on Host Iron Absorption
Led by Cornell University · Updated on 2025-02-24
120
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research investigates how different types of dietary iron, heme from animal products and non-heme from both plants and animals, affect the gut microbiome and iron absorption in healthy adults aged 18 to 40. The study aims to understand how the gut bacteria and dietary iron interact, especially as more people adopt plant-based diets that reduce heme iron intake. Researchers will explore how these changes influence individual differences in iron absorption, addressing important gaps in knowledge about iron and gut microbes in humans. Participants will be recruited based on their usual diet, either plant-based or containing animal protein. Each participant will consume a dose of stable isotope-labeled iron (57Fe) in a fasting state, followed by two standardized meals. Two weeks later, blood samples will be taken to measure how much 57Fe has been absorbed into red blood cells. Around the time they consume the iron dose, participants will also provide a stool sample for detailed gut microbiome analysis using DNA sequencing methods. During the study, various assessments will be done including measuring blood markers like hemoglobin, ferritin, transferrin receptor, and hematocrit at baseline. Dietary information will be collected both at baseline and on the day before iron dosing. The gut microbiome composition will be analyzed from stool samples. The primary outcomes focus on the percentage of non-heme iron absorbed after two weeks and baseline blood and dietary measures. This observational study is conducted by Cornell University and involves healthy adult volunteers with no major health issues affecting iron metabolism.
CONDITIONS
Brief Title
Heme and Non-heme Iron Intakes, Gut Microbiota, and Influence on Host Iron Absorption
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults
- Age between 18 and 40 years
- Non-smoking
- Not currently taking vitamin, mineral, prebiotic, or probiotic supplements
- Females must be premenopausal and not pregnant or lactating
- No preexisting medical complications such as eating disorders, hemoglobinopathies, malabsorption diseases, steroid use, substance abuse, or medications affecting iron homeostasis
- Body mass index (BMI) between 18 and 27 kg/m2
You will not qualify if you...
- Body mass index (BMI) less than 18 or greater than 27 kg/m2
- Age under 18 or over 40 years
- Smoking
- Pregnancy or lactating
- Gastrointestinal disorders, malabsorption diseases, hemoglobinopathies, dietary restrictions, steroid use, or medications impacting iron status or inflammation
- Current use of vitamin, mineral, prebiotic, or probiotic supplements
- Recent antibiotic treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 weeks
Participants consume a stable iron isotope dose and provide stool and blood samples to assess iron absorption and gut microbiome composition.
1 visit for iron dosing and stool sample collection, 1 follow-up visit for blood sample collection
Trial Site Locations
Total: 1 location
1
Cornell University
Ithaca, New York, United States, 14853
Actively Recruiting
Research Team
K
Kimberly O O'Brien, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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