Glycoprotein Matrix-Bound Iron Improves Iron Absorption
Palo Alto (17 mi)Age: 18 - 65
Sex: Any
Travel: May be covered
Time Reimbursement: Varies
Trial Phase: N/A
Waitlist Available
Sponsor: University of Mary Hardin-Baylor
No Placebo Group
Trial Summary
What is the purpose of this trial?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.
Eligibility Criteria
Treatment Details
3Treatment groups
Experimental Treatment
Group I: glycoprotein matrix ironExperimental Treatment1 Intervention
Acute glycoprotein matrix iron was ingested to assess blood appearance levels from pre and at 30-, 60-, 90-, 120-, 180-, 240-, 300-, 360-, 420-, and 480-minutes post-ingestion.
Group II: ferrous fumarate ironExperimental Treatment1 Intervention
Acute ferrous fumarate iron was ingested to assess blood appearance levels from pre and at 30-, 60-, 90-, 120-, 180-, 240-, 300-, 360-, 420-, and 480-minutes post-ingestion.
Group III: ferrous bisglycinate chelate ironExperimental Treatment1 Intervention
Acute ferrous bisglycinate chelate iron was ingested to assess blood appearance levels from pre and at 30-, 60-, 90-, 120-, 180-, 240-, 300-, 360-, 420-, and 480-minutes post-ingestion.
Find a clinic near you
Research locations nearbySelect from list below to view details:
Human Performance LabBelton, TX
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Who is running the clinical trial?
University of Mary Hardin-BaylorLead Sponsor
Pharmachem InnovationsCollaborator