RecruitingNot ApplicableNCT07315282

The Effect of Oral Iron Supplements on Insulin and Glucose Metabolism in Overweight and Obese Women


Sponsor

Nicole Stoffel

Enrollment

70 participants

Start Date

Dec 23, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The study will be a randomized, double-blind, 17-day metabolic intervention trial including 14 days of high-dose or low-dose iron supplementation. A total of 70 overweight or obese (OW/OB) women will be enrolled. Participants will be individually randomized into either the high-iron or low-iron group. Women in the low-iron group will receive 15 mg of iron as ferrous fumarate daily for 14 days, while women in the high-iron group will receive 195 mg of iron as ferrous sulfate daily for 14 days. The study consists of three visits in total. On Day 0, a fasting blood sample will be collected and an OGTT will be performed, with additional blood samples collected at 1 hour and 2 hours post-OGTT. The OGTT will be repeated on Day 14, after 14 days of oral iron supplementation, and again on Day 17, four days after oral iron supplementation has been stopped


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying 15 mg iron daily and 195 mg iron daily for people with overweight and obese women. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENT195 mg iron daily

3 x 65 mg iron as ferrous sulfate

DIETARY_SUPPLEMENT15 mg iron daily

3 x 5 mg iron as ferrous sulfate


Locations(1)

American University of Beirut

Beirut, Lebanon

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NCT07315282


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