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Clinical Trial Summary

This project is a randomized crossover trial examining the pharmacokinetic profiles of standard and liposomal multivitamin/mineral (MVM) formulations in healthy adults. Each participant will complete two research visits, which will be identical except for which MVM product is consumed. At each visit, participants will report to the laboratory after an overnight fast. After a baseline blood sample is collected, the MVM product will be consumed alongside a standardized breakfast. At 2-, 4-, and 6-hours post-ingestion, additional blood samples will be collected. Concentrations of representative fat-soluble and water-soluble vitamins, as well as representative minerals, will be analyzed to determine whether differential nutrient absorption is observed with the liposomal MVM as compared to the standard MVM product. The results of this study will provide information about a novel liposomal MVM formulation and will inform future research and commercial applications of this technology.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05060367
Study type Interventional
Source Texas Tech University
Contact Grant M Tinsley, PhD
Phone 8068345895
Email [email protected]
Status Recruiting
Phase N/A
Start date September 16, 2021
Completion date December 2021

See also
  Status Clinical Trial Phase
Completed NCT00868738 - Evaluation of Calcium, Vitamin D, Magnesium, and Zinc Absorption in Children N/A