Glycoprotein Matrix-Bound Iron Improves Iron Absorption
Completed · Not applicable
Conditions studied: Evaluation of Bioavailability of Supplemental Forms of Iron
In brief
A double-blind, randomized crossover study was conducted that evaluated absorption kinetics of 3 forms of dietary supplement iron by measuring iron levels in the blood after acute ingestion.
Key facts
- Study ID
- NCT06738199
- Run by
- University of Mary Hardin-Baylor
- People needed
- 17
- Starts
- 2024-02-01
- Expected to finish
- 2024-04-22
- Last updated by the study team
- 2024-12-17
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Participants had to have a normal body weight [body mass index (BMI) of 19-24.99 kg/m2] and engage in recreational physical activity, as defined by the American College of Sports Medicine guidelines.
- Participants must be healthy and have no diagnosed chronic disease conditions
You may not qualify if…
- Participants were not allowed to consume any nutritional supplements known to affect the measures of the current study for at least 6 weeks prior to participation, including pro-, post- and prebiotics, as well as digestive enzymes.
- Individuals who were currently being treated for or diagnosed with a gastrointestinal, cardiac, respiratory, circulatory, musculoskeletal, metabolic, immune, autoimmune, psychiatric, hematological, neurological, or endocrinological disorder.
- Participants whose body mass had deviated by more than 2% in the previous 30 days
- Participants who were unwilling to abstain from alcohol, nicotine, and caffeine for 12 hours prior to each visit.
Where it is running
- Human Performance Lab — Belton, Texas, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.